• 2 Citations
  • 1 h-Index
20182019
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Research Output 2018 2019

  • 2 Citations
  • 1 h-Index
  • 2 Article
2019
2 Citations (Scopus)

A nonsense mutation in myelin protein zero causes congenital hypomyelination neuropathy through altered P0 membrane targeting and gain of abnormal function

Fratta, P., Ornaghi, F., Dati, G., Zambroni, D., Saveri, P., Belin, S., D'Adamo, P., Shy, M., Quattrini, A., Laura Feltri, M. & Wrabetz, L., Jan 1 2019, In : Human Molecular Genetics. 28, 1, p. 124-132 9 p.

Research output: Contribution to journalArticle

Myelin P0 Protein
Nonsense Codon
Phenotype
Membranes
Myelin Sheath
2018

A dual role for Integrin α6β4 in modulating hereditary neuropathy with liability to pressure palsies

Poitelon, Y., Matafora, V., Silvestri, N., Zambroni, D., McGarry, C., Serghany, N., Rush, T., Vizzuso, D., Court, FA., Bachi, A., Wrabetz, L. & Feltri, ML., 2018, In : Journal of Neurochemistry. 145, 3, p. 245-257 13 p.

Research output: Contribution to journalArticle

Myelin Proteins
Integrins
Paralysis
Myelin Sheath
Pressure