Fratta, P; Ornaghi, F; Dati, G; Zambroni, D; Saveri, P; Belin, S; D'Adamo, P; ... Wrabetz, L; + view all Fratta, P; Ornaghi, F; Dati, G; Zambroni, D; Saveri, P; Belin, S; D'Adamo, P; Shy, M; Quattrini, A; Laura Feltri, M; Wrabetz, L; - view fewer (2018) A nonsense mutation in Myelin Protein Zero causes congenital hypomyelination neuropathy through altered P0 membrane targeting and gain of abnormal function. Human Molecular Genetics 10.1093/hmg/ddy336 . (In press). Green open access
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Παρασκευή 12 Οκτωβρίου 2018
A nonsense mutation in Myelin Protein Zero causes congenital hypomyelination neuropathy through altered P0 membrane targeting and gain of abnormal function
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