Molecular Diagnosis of Mitochondrial Disorders

J. Finsterer; H. F. Harbo; J. Baets; C. Van Broeckhoven; S. Di Donato; B. Fontaine; P. De Jonghe; A. Lossos; T. Lynch; C. Mariotti; L. Schöls; A. Spinazzola; Z. Szolnoki; S. J. Tabrizi; C. Tallaksen; M. Zeviani; J. M. Burgunder; T. Gasser

doi:10.1002/9781444346268.ch5

Molecular Diagnosis of Mitochondrial Disorders

J. Finsterer, H. F. Harbo, J. Baets, C. Van Broeckhoven, S. Di Donato, B. Fontaine, P. De Jonghe, A. Lossos, T. Lynch, C. Mariotti, L. Schöls, A. Spinazzola, Z. Szolnoki, S. J. Tabrizi, C. Tallaksen, M. Zeviani, J. M. Burgunder, T. Gasser

Fondazione IRCCS Istituto Neurologico "C. Besta"

Research output: Chapter in Book/Report/Conference proceeding › Chapter

Original language	English
Title of host publication	European Handbook of Neurological Management
Publisher	Wiley-Blackwell
Pages	61-72
Number of pages	12
Volume	2
ISBN (Print)	9781405185349
DOIs	https://doi.org/10.1002/9781444346268.ch5
Publication status	Published - Sep 21 2011

Keywords

Encephalomyopathies
Hereditary disease
Metabolic myopathies
Mitochondrial myopathy
Molecular genetics

ASJC Scopus subject areas

Neuroscience(all)

Access to Document

10.1002/9781444346268.ch5

Cite this

Finsterer, J., Harbo, H. F., Baets, J., Van Broeckhoven, C., Di Donato, S., Fontaine, B., De Jonghe, P., Lossos, A., Lynch, T., Mariotti, C., Schöls, L., Spinazzola, A., Szolnoki, Z., Tabrizi, S. J., Tallaksen, C., Zeviani, M., Burgunder, J. M., & Gasser, T. (2011). Molecular Diagnosis of Mitochondrial Disorders. In European Handbook of Neurological Management (Vol. 2, pp. 61-72). Wiley-Blackwell. https://doi.org/10.1002/9781444346268.ch5

Molecular Diagnosis of Mitochondrial Disorders. / Finsterer, J.; Harbo, H. F.; Baets, J.; Van Broeckhoven, C.; Di Donato, S.; Fontaine, B.; De Jonghe, P.; Lossos, A.; Lynch, T.; Mariotti, C.; Schöls, L.; Spinazzola, A.; Szolnoki, Z.; Tabrizi, S. J.; Tallaksen, C.; Zeviani, M.; Burgunder, J. M.; Gasser, T.

European Handbook of Neurological Management. Vol. 2 Wiley-Blackwell, 2011. p. 61-72.

Research output: Chapter in Book/Report/Conference proceeding › Chapter

Finsterer, J, Harbo, HF, Baets, J, Van Broeckhoven, C, Di Donato, S, Fontaine, B, De Jonghe, P, Lossos, A, Lynch, T, Mariotti, C, Schöls, L, Spinazzola, A, Szolnoki, Z, Tabrizi, SJ, Tallaksen, C, Zeviani, M, Burgunder, JM & Gasser, T 2011, Molecular Diagnosis of Mitochondrial Disorders. in European Handbook of Neurological Management. vol. 2, Wiley-Blackwell, pp. 61-72. https://doi.org/10.1002/9781444346268.ch5

Finsterer, J. ; Harbo, H. F. ; Baets, J. ; Van Broeckhoven, C. ; Di Donato, S. ; Fontaine, B. ; De Jonghe, P. ; Lossos, A. ; Lynch, T. ; Mariotti, C. ; Schöls, L. ; Spinazzola, A. ; Szolnoki, Z. ; Tabrizi, S. J. ; Tallaksen, C. ; Zeviani, M. ; Burgunder, J. M. ; Gasser, T. / Molecular Diagnosis of Mitochondrial Disorders. European Handbook of Neurological Management. Vol. 2 Wiley-Blackwell, 2011. pp. 61-72

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