• 1005 Citations
  • 17 h-Index
20092019
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Research Output 2009 2019

  • 1005 Citations
  • 17 h-Index
  • 43 Article
  • 1 Letter
2019

Novel mutations in DNA2 associated with myopathy and mtDNA instability

Ronchi, D., Liu, C., Caporali, L., Piga, D., Li, H., Tagliavini, F., Valentino, M. L., Ferrò, M. T., Bini, P., Zheng, L., Carelli, V., Shen, B. & Comi, G. P., 2019, In : Annals of Clinical and Translational Neurology. 6, 9, p. 1893-1899

Research output: Contribution to journalArticle

Open Access
Muscular Diseases
Mitochondrial DNA
Mutation
Mitochondrial Myopathies
Nuclear Proteins

Novel mutations in DNA2 associated with myopathy and mtDNA instability

Ronchi, D., Liu, C., Caporali, L., Piga, D., Li, H., Tagliavini, F., Valentino, M. L., Ferrò, M. T., Bini, P., Zheng, L., Carelli, V., Shen, B. & Comi, G. P., Sep 2019, In : Annals of Clinical and Translational Neurology. 6, 9, p. 1893-1899 7 p.

Research output: Contribution to journalArticle

SCN1A mutations in focal epilepsy with auditory features: widening the spectrum of GEFS plus

Bisulli, F., Licchetta, L., Baldassari, S., Muccioli, L., Marconi, C., Cantalupo, G., Myers, C., Menghi, V., Minardi, R., Caporali, L., Marini, C., Guerrini, R., Mefford, H. C., Tinuper, P. & Pippucci, T., Apr 2019, In : Epileptic Disorders. 21, 2, p. 185-191 7 p.

Research output: Contribution to journalArticle

Partial Epilepsy
Epilepsy
Mutation
Febrile Seizures
Nuclear Family
2018

Cerebral mitochondrial microangiopathy leads to leukoencephalopathy in mitochondrial neurogastrointestinal encephalopathy

Gramegna, L. L., Pisano, A., Testa, C., Manners, D. N., D'Angelo, R., Boschetti, E., Giancola, F., Pironi, L., Caporali, L., Capristo, M., Valentino, M. L., Plazzi, G., Casali, C., Dotti, M. T., Cenacchi, G., Hirano, M., Giordano, C., Parchi, P., Rinaldi, R., De Giorgio, R. & 3 others, Lodi, R., Carelli, V. & Tonon, C., Mar 1 2018, In : American Journal of Neuroradiology. 39, 3, p. 427-434 8 p.

Research output: Contribution to journalArticle

Cerebral Small Vessel Diseases
Leukoencephalopathies
Thymidine Phosphorylase
Brain
DNA Replication

Complex II phosphorylation is triggered by unbalanced redox homeostasis in cells lacking complex III

Tropeano, C. V., Fiori, J., Carelli, V., Caporali, L., Daldal, F., Ghelli, A. M. & Rugolo, M., Mar 1 2018, In : Biochimica et Biophysica Acta - Bioenergetics. 1859, 3, p. 182-190 9 p.

Research output: Contribution to journalArticle

Phosphorylation
Electron Transport Complex III
Oxidation-Reduction
Homeostasis
Tyrosine

Deciphering OPA1 mutations pathogenicity by combined analysis of human, mouse and yeast cell models

Del Dotto, V., Fogazza, M., Musiani, F., Maresca, A., Aleo, S. J., Caporali, L., La Morgia, C., Nolli, C., Lodi, T., Goffrini, P., Chan, D., Carelli, V., Rugolo, M., Baruffini, E. & Zanna, C., Oct 1 2018, In : Biochimica et Biophysica Acta - Molecular Basis of Disease. 1864, 10, p. 3496-3514 19 p.

Research output: Contribution to journalArticle

Autosomal Dominant Optic Atrophy
Virulence
Yeasts
Mutation
Mitochondrial DNA

Haplogroup J mitogenomes are the most sensitive to the pesticide rotenone: Relevance for human diseases

Strobbe, D., Caporali, L., Iommarini, L., Maresca, A., Montopoli, M., Martinuzzi, A., Achilli, A., Olivieri, A., Torroni, A., Carelli, V. & Ghelli, A., Jun 2018, In : Neurobiology of Disease. 114, p. 129-139 11 p.

Research output: Contribution to journalArticle

Rotenone
Mitochondrial DNA
Pesticides
Leber's Hereditary Optic Atrophy
Parkinson Disease

Identification of rare genetic variants in Italian patients with dementia by targeted gene sequencing

Bartoletti-Stella, A., Baiardi, S., Stanzani-Maserati, M., Piras, S., Caffarra, P., Raggi, A., Pantieri, R., Baldassari, S., Caporali, L., Abu-Rumeileh, S., Linarello, S., Liguori, R., Parchi, P. & Capellari, S., Jun 1 2018, In : Neurobiology of Aging. 66, p. 180.e23-180.e31

Research output: Contribution to journalArticle

Dementia
Genes
Presenilin-2
Presenilin-1
Serpins

Peculiar combinations of individually non-pathogenic missense mitochondrial DNA variants cause low penetrance Leber’s hereditary optic neuropathy

Caporali, L., Iommarini, L., La Morgia, C., Olivieri, A., Achilli, A., Maresca, A., Valentino, M. L., Capristo, M., Tagliavini, F., Del Dotto, V., Zanna, C., Liguori, R., Barboni, P., Carbonelli, M., Cocetta, V., Montopoli, M., Martinuzzi, A., Cenacchi, G., De Michele, G., Testa, F. & 5 others, Nesti, A., Simonelli, F., Porcelli, A. M., Torroni, A. & Carelli, V., 2018, In : PLoS Genetics. 14, 2, e1007210.

Research output: Contribution to journalArticle

Pharmacological Inhibition of Necroptosis Protects from Dopaminergic Neuronal Cell Death in Parkinson's Disease Models

Iannielli, A., Bido, S., Folladori, L., Segnali, A., Cancellieri, C., Maresca, A., Massimino, L., Rubio, A., Morabito, G., Caporali, L., Tagliavini, F., Musumeci, O., Gregato, G., Bezard, E., Carelli, V., Tiranti, V. & Broccoli, V., Feb 2018, In : Cell Reports. 22, 8, p. 2066-2079 14 p.

Research output: Contribution to journalArticle

Pharmacological Inhibition of Necroptosis Protects from Dopaminergic Neuronal Cell Death in Parkinson's Disease Models

Iannielli, A., Bido, S., Folladori, L., Segnali, A., Cancellieri, C., Maresca, A., Massimino, L., Rubio, A., Morabito, G., Caporali, L., Tagliavini, F., Musumeci, O., Gregato, G., Bezard, E., Carelli, V., Tiranti, V. & Broccoli, V., Feb 20 2018, In : Cell Reports. 22, 8, p. 2094-2106 13 p.

Research output: Contribution to journalArticle

Cell death
Parkinson Disease
Cell Death
Pharmacology
Mitochondrial Dynamics
2017
Leber's Hereditary Optic Atrophy
Optic Nerve Diseases
Penetrance
Mitochondrial DNA
Autosomal Dominant Optic Atrophy

Liver transplant reverses biochemical imbalance in mitochondrial neurogastrointestinal encephalomyopathy

D'Angelo, R., Rinaldi, R., Pironi, L., Dotti, M. T., Pinna, D. A., Boschetti, E., Capristo, M., Mohamed, S., Contin, M., Caporali, L., Carelli, V. & De Giorgio, R., 2017, In : Mitochondrion. 34, p. 101-102

Research output: Contribution to journalArticle

OPA1 Isoforms in the Hierarchical Organization of Mitochondrial Functions

Del Dotto, V., Mishra, P., Vidoni, S., Fogazza, M., Maresca, A., Caporali, L., McCaffery, J. M., Cappelletti, M., Baruffini, E., Lenaers, G., Chan, D., Rugolo, M., Carelli, V. & Zanna, C., Jun 20 2017, In : Cell Reports. 19, 12, p. 2557-2571 15 p.

Research output: Contribution to journalArticle

Protein Isoforms
Mitochondrial Dynamics
Mitochondrial DNA
Fusion reactions
Haploinsufficiency

Somatic mutation profiling of hobnail variant of papillary thyroid carcinoma

Morandi, L., Righi, A., Maletta, F., Rucci, P., Pagni, F., Gallo, M., Rossi, S., Caporali, L., Sapino, A., Lloyd, R. V. & Asioli, S., 2017, In : Endocrine-Related Cancer. 24, 2, p. 107-117 11 p.

Research output: Contribution to journalArticle

Somatic mutation profiling of hobnail variant of papillary thyroid carcinoma

Morandi, L., Righi, A., Maletta, F., Rucci, P., Pagni, F., Gallo, M., Rossi, S., Caporali, L., Sapino, A., Lloyd, R. V. & Asioli, S., 2017, In : Endocrine-Related Cancer. 24, 2, p. 107-117 11 p.

Research output: Contribution to journalArticle

Mutation
Neoplasms
Neoplasm Metastasis
Molecular Typing
Papillary Thyroid cancer

Somatic mutation profiling of hobnail variant of papillary thyroid carcinoma.

Morandi, L., Righi, A., Maletta, F., Rucci, P., Pagni, F., Gallo, M., Rossi, S., Caporali, L., Sapino, A., Lloyd, R. V. & Asioli, S., Feb 1 2017, In : Endocrine-Related Cancer. 24, p. 107-117 11 p.

Research output: Contribution to journalArticle

Mutation
Neoplasms
Neoplasm Metastasis
Molecular Typing
Papillary Thyroid cancer

Whole Mitogenomes Reveal the History of Swamp Buffalo: Initially Shaped by Glacial Periods and Eventually Modelled by Domestication

Wang, S., Chen, N., Capodiferro, M. R., Zhang, T., Lancioni, H., Zhang, H., Miao, Y., Chanthakhoun, V., Wanapat, M., Yindee, M., Zhang, Y., Lu, H., Caporali, L., Dang, R., Huang, Y., Lan, X., Plath, M., Chen, H., Lenstra, J. A., Achilli, A. & 1 others, Lei, C., Dec 1 2017, In : Scientific Reports. 7, 1, 4708.

Research output: Contribution to journalArticle

domestication
swamp
history
demographic history
population bottleneck
2016

ITA-MNGIE: an Italian regional and national survey for mitochondrial neuro-gastro-intestinal encephalomyopathy

D’Angelo, R., Rinaldi, R., Carelli, V., Boschetti, E., Caporali, L., Capristo, M., Casali, C., Cenacchi, G., Gramegna, L. L., Lodi, R., Pinna, A. D., Pironi, L., Stanzani, M., Tonon, C., D’Alessandro, R. & de Giorgio, R., 2016, In : Neurological Sciences. 37, p. 1149-1151 3 p.

Research output: Contribution to journalArticle

Thymidine Phosphorylase
Italy
Cachexia
Hematopoietic Stem Cell Transplantation
Neurologic Manifestations

Liver transplantation for mitochondrial neurogastrointestinal encephalomyopathy

De Giorgio, R., Pironi, L., Rinaldi, R., Boschetti, E., Caporali, L., Capristo, M., Casali, C., Cenacchi, G., Contin, M., D'Angelo, R., D'Errico, A., Gramegna, L. L., Lodi, R., Maresca, A., Mohamed, S., Morelli, M. C., Papa, V., Tonon, C., Tugnoli, V., Carelli, V. & 2 others, D'Alessandro, R. & Pinna, A. D., Sep 1 2016, In : Annals of Neurology. 80, 3, p. 448-455 8 p.

Research output: Contribution to journalArticle

Mitochondrial Encephalomyopathies
Thymidine Phosphorylase
Liver Transplantation
Poisons
Nucleosides

Pharmacogenetics and treatment response in narcolepsy type 1: Relevance of the polymorphisms of the drug transporter gene abcb1

Moresco, M., Riccardi, L. N., Pizza, F., Zenesini, C., Caporali, L., Plazzi, G. & Pelotti, S., 2016, In : Clinical Neuropharmacology. 39, 1, p. 18-23 6 p.

Research output: Contribution to journalArticle

Pharmacogenetics
Pharmaceutical Preparations
Genes
Cataplexy
Therapeutics

Reply: Both mitochondrial DNA and mitonuclear gene mutations cause hearing loss through cochlear dysfunction

Santarelli, R., Cama, E., Scimemi, P., La Morgia, C., Caporali, L., Valentino, M. L., Liguori, R. & Carelli, V., 2016, In : Brain. 139, 6, p. e34

Research output: Contribution to journalLetter

2015

'Behr syndrome' with OPA1 compound heterozygote mutations

Carelli, V., Sabatelli, M., Carrozzo, R., Rizza, T., Schimpf, S., Wissinger, B., Zanna, C., Rugolo, M., La Morgia, C., Caporali, L., Carbonelli, M., Barboni, P., Tonon, C., Lodi, R. & Bertini, E., Jan 1 2015, In : Brain. 138, p. e321

Research output: Contribution to journalArticle

Diffusion tensor imaging mapping of brain white matter pathology in mitochondrial optic neuropathies

Manners, D. N., Rizzo, G., La Morgia, C., Tonon, C., Testa, C., Barboni, P., Malucelli, E., Valentino, M. L., Caporali, L., Strobbe, D., Carelli, V. & Lodi, R., Jul 1 2015, In : American Journal of Neuroradiology. 36, 7, p. 1259-1265 7 p.

Research output: Contribution to journalArticle

Brain Mapping
Autosomal Dominant Optic Atrophy
Optic Nerve Diseases
Diffusion Tensor Imaging
Leber's Hereditary Optic Atrophy

DNA methyltransferase 1 mutations and mitochondrial pathology: Is mtDNA methylated?

Maresca, A., Zaffagnini, M., Caporali, L., Carelli, V. & Zanna, C., 2015, In : Frontiers in Genetics. 5, FEB, 90.

Research output: Contribution to journalArticle

Methyltransferases
Mitochondrial DNA
Pathology
Mutation
DNA

Mitochondria: Biogenesis and mitophagy balance in segregation and clonal expansion of mitochondrial DNA mutations

Carelli, V., Maresca, A., Caporali, L., Trifunov, S., Zanna, C. & Rugolo, M., Jun 1 2015, In : International Journal of Biochemistry and Cell Biology. 63, p. 21-24 4 p.

Research output: Contribution to journalArticle

Mitochondrial Degradation
Mitochondria
Mitochondrial DNA
Mutation
Genes

Mutations in SLC25A46, encoding a UGO1-like protein, cause an optic atrophy spectrum disorder

Abrams, A. J., Hufnagel, R. B., Rebelo, A., Zanna, C., Patel, N., Gonzalez, M. A., Campeanu, I. J., Griffin, L. B., Groenewald, S., Strickland, A. V., Tao, F., Speziani, F., Abreu, L., Schüle, R., Caporali, L., La Morgia, C., Maresca, A., Liguori, R., Lodi, R., Ahmed, Z. M. & 20 others, Sund, K. L., Wang, X., Krueger, L. A., Peng, Y., Prada, C. E., Prows, C. A., Schorry, E. K., Antonellis, A., Zimmerman, H. H., Abdul-Rahman, O. A., Yang, Y., Downes, S. M., Prince, J., Fontanesi, F., Barrientos, A., Németh, A. H., Carelli, V., Huang, T., Zuchner, S. & Dallman, J. E., Aug 30 2015, In : Nature Genetics. 47, 8, p. 926-932 7 p.

Research output: Contribution to journalArticle

Mitochondrial Dynamics
Optic Atrophy
Autosomal Dominant Optic Atrophy
Exome
Mutation

OPA1-related auditory neuropathy: Site of lesion and outcome of cochlear implantation

Santarelli, R., Rossi, R., Scimemi, P., Cama, E., Valentino, M. L., La Morgia, C., Caporali, L., Liguori, R., Magnavita, V., Monteleone, A., Biscaro, A., Arslan, E. & Carelli, V., 2015, In : Brain. 138, 3, p. 563-576 14 p.

Research output: Contribution to journalArticle

Cochlear Implantation
Speech Perception
Missense Mutation
Cochlear Nerve
Hearing

Syndromic parkinsonism and dementia associated with OPA1 missense mutations

Carelli, V., Musumeci, O., Caporali, L., Zanna, C., La Morgia, C., Del Dotto, V., Porcelli, A. M., Rugolo, M., Valentino, M. L., Iommarini, L., Maresca, A., Barboni, P., Carbonelli, M., Trombetta, C., Valente, E. M., Patergnani, S., Giorgi, C., Pinton, P., Rizzo, G., Tonon, C. & 6 others, Lodi, R., Avoni, P., Liguori, R., Baruzzi, A., Toscano, A. & Zeviani, M., Jul 1 2015, In : Annals of Neurology. 78, 1, p. 21-38 18 p.

Research output: Contribution to journalArticle

Mitochondrial Dynamics
Parkinsonian Disorders
Missense Mutation
Mitochondrial DNA
Chronic Progressive External Ophthalmoplegia
2014

A Novel in-Frame 18-bp Microdeletion in MT-CYB Causes a Multisystem Disorder with Prominent Exercise Intolerance

Carossa, V., Ghelli, A., Tropeano, C. V., Valentino, M. L., Iommarini, L., Maresca, A., Caporali, L., La Morgia, C., Liguori, R., Barboni, P., Carbonelli, M., Rizzo, G., Tonon, C., Lodi, R., Martinuzzi, A., De Nardo, V., Rugolo, M., Ferretti, L., Gandini, F., Pala, M. & 4 others, Achilli, A., Olivieri, A., Torroni, A. & Carelli, V., 2014, In : Human Mutation. 35, 8, p. 954-958 5 p.

Research output: Contribution to journalArticle

Mitochondrial DNA
Retinal Dystrophies
Exercise
Cytochromes b
Electron Transport Complex III

Association of the mtDNA m.4171C>A/MT-ND1 mutation with both optic neuropathy and bilateral brainstem lesions

La Morgia, C., Caporali, L., Gandini, F., Olivieri, A., Toni, F., Nassetti, S., Brunetto, D., Stipa, C., Scaduto, C., Parmeggiani, A., Tonon, C., Lodi, R., Torroni, A. & Carelli, V., May 28 2014, In : BMC Neurology. 14, 1, 116.

Research output: Contribution to journalArticle

Leber's Hereditary Optic Atrophy
Optic Nerve Diseases
Mitochondrial DNA
Brain Stem
Mutation

Early macular retinal ganglion cell loss in dominant optic atrophy: Genotype-phenotype correlation

Barboni, P., Savini, G., Cascavilla, M. L., Caporali, L., Milesi, J., Borrelli, E., La Morgia, C., Valentino, M. L., Triolo, G., Lembo, A., Carta, A., De Negri, A., Sadun, F., Rizzo, G., Parisi, V., Pierro, L., Bianchi Marzoli, S., Zeviani, M., Sadun, A. A., Bandello, F. & 1 others, Carelli, V., 2014, In : American Journal of Ophthalmology. 158, 3

Research output: Contribution to journalArticle

Autosomal Dominant Optic Atrophy
Retinal Ganglion Cells
Genetic Association Studies
Nerve Fibers
Ganglia

Efficient mitochondrial biogenesis drives incomplete penetrance in Leber's hereditary optic neuropathy

Giordano, C., Iommarini, L., Giordano, L., Maresca, A., Pisano, A., Valentino, M. L., Caporali, L., Liguori, R., Deceglie, S., Roberti, M., Fanelli, F., Fracasso, F., Ross-Cisneros, F. N., D'adamo, P., Hudson, G., Pyle, A., Yu-Wai-Man, P., Chinnery, P. F., Zeviani, M., Salomao, S. R. & 15 others, Berezovsky, A., Belfort, R., Ventura, D. F., Moraes, M., Moraes Filho, M., Barboni, P., Sadun, F., De Negri, A., Sadun, A. A., Tancredi, A., Mancini, M., D'amati, G., Loguercio Polosa, P., Cantatore, P. & Carelli, V., 2014, In : Brain. 137, 2, p. 335-353 19 p.

Research output: Contribution to journalArticle

Leber's Hereditary Optic Atrophy
Penetrance
Organelle Biogenesis
Mitochondrial DNA
Mutation

Genetic basis of mitochondrial optic neuropathies

Maresca, A., Caporali, L., Strobbe, D., Zanna, C., Malavolta, D., La Morgia, C., Valentino, M. L. & Carelli, V., Mar 1 2014, In : Current Molecular Medicine. 14, 8, p. 985-992 8 p.

Research output: Contribution to journalArticle

Leber's Hereditary Optic Atrophy
Optic Nerve Diseases
Optics
Autosomal Dominant Optic Atrophy
Penetrance
Thymidine Phosphorylase
Deoxyuridine
Thymidine
Assays
High Pressure Liquid Chromatography
2013

Cybrid studies establish the causal link between the mtDNA m.3890G>A/MT-ND1 mutation and optic atrophy with bilateral brainstem lesions

Caporali, L., Ghelli, A. M., Iommarini, L., Maresca, A., Valentino, M. L., La Morgia, C., Liguori, R., Zanna, C., Barboni, P., De Nardo, V., Martinuzzi, A., Rizzo, G., Tonon, C., Lodi, R., Calvaruso, M. A., Cappelletti, M., Porcelli, A. M., Achilli, A., Pala, M., Torroni, A. & 1 others, Carelli, V., Mar 2013, In : Biochimica et Biophysica Acta - Molecular Basis of Disease. 1832, 3, p. 445-452 8 p.

Research output: Contribution to journalArticle

Optic Atrophy
Mitochondrial DNA
Brain Stem
Mutation
Leber's Hereditary Optic Atrophy

Idebenone treatment in patients with OPA1-mutant dominant optic atrophy

Barboni, P., Valentino, M. L., La Morgia, C., Carbonelli, M., Savini, G., De Negri, A., Simonelli, F., Sadun, F., Caporali, L., Maresca, A., Liguori, R., Baruzzi, A., Zeviani, M. & Carelli, V., 2013, In : Brain. 136, 2

Research output: Contribution to journalArticle

Oncocytic glioblastoma: A glioblastoma showing oncocytic changes and increased mitochondrial DNA copy number

Marucci, G., Maresca, A., Caporali, L., Farnedi, A., Betts, C. M., Morandi, L., De Biase, D., Cerasoli, S., Foschini, M. P., Bonora, E., Vidone, M., Romeo, G., Perli, E., Giordano, C., D'Amati, G., Gasparre, G., Baruzzi, A., Carelli, V. & Eusebi, V., Sep 2013, In : Human Pathology. 44, 9, p. 1867-1876 10 p.

Research output: Contribution to journalArticle

Glioblastoma
Mitochondrial DNA
Cytoplasm
Mitochondria
Neoplasms

The optic nerve: A "mito-window" on mitochondrial neurodegeneration

Maresca, A., la Morgia, C., Caporali, L., Valentino, M. L. & Carelli, V., Jul 2013, In : Molecular and Cellular Neuroscience. 55, p. 62-76 15 p.

Research output: Contribution to journalArticle

Optic Nerve
Neurodegenerative Diseases
Optic Atrophy
Leber's Hereditary Optic Atrophy
Mitochondrial Diseases
2012

Revisiting the issue of mitochondrial dna contentinopticmitochondriopathies

Iommarini, L., Maresca, A., Caporali, L., Valentino, M. L., Liguori, R., Giordano, C. & Carelli, V., Oct 2 2012, In : Neurology. 79, 14, p. 1517-1519 3 p.

Research output: Contribution to journalArticle

2010

Multi-system neurological disease is common in patients with OPA1 mutations

Yu-Wai-Man, P., Griffiths, P. G., Gorman, G. S., Lourenco, C. M., Wright, A. F., Auer-Grumbach, M., Toscano, A., Musumeci, O., Valentino, M. L., Caporali, L., Lamperti, C., Tallaksen, C. M., Duffey, P., Miller, J., Whittaker, R. G., Baker, M. R., Jackson, M. J., Clarke, M. P., Dhillon, B., Czermin, B. & 16 others, Stewart, J. D., Hudson, G., Reynier, P., Bonneau, D., Marques, W., Lenaers, G., McFarland, R., Taylor, R. W., Turnbull, D. M., Votruba, M., Zeviani, M., Carelli, V., Bindoff, L. A., Horvath, R., Amati-Bonneau, P. & Chinnery, P. F., Mar 2010, In : Brain. 133, 3, p. 771-786 16 p.

Research output: Contribution to journalArticle

Autosomal Dominant Optic Atrophy
Mutation
Electron Transport Complex IV
Mitochondrial DNA
Odds Ratio

Variation in OPA1 does not explain the incomplete penetrance of Leber hereditary optic neuropathy

Hudson, G., Yu-Wai-Man, P., Griffiths, P. G., Caporali, L., Salomao, S. S., Berezovsky, A., Carelli, V., Zeviani, M. & Chinnery, P. F., 2010, In : Molecular Vision. 16, p. 2760-2764 5 p.

Research output: Contribution to journalArticle

Autosomal Dominant Optic Atrophy
Leber's Hereditary Optic Atrophy
Penetrance
Mitochondrial DNA
Blindness
2009

Terminal-restriction fragment length polymorphism analysis of biphenyl dioxygenase genes from a polychlorinated biphenyl-polluted soil

Capodicasa, S., Fedi, S., Carnevali, M., Caporali, L., Viti, C., Fava, F. & Zannoni, D., Dec 2009, In : Research in Microbiology. 160, 10, p. 742-750 9 p.

Research output: Contribution to journalArticle

Dioxygenases
biphenyl-2,3-dioxygenase
Polychlorinated Biphenyls
Restriction Fragment Length Polymorphisms
Soil