Different Intracellular Pathomechanisms Produce Diverse Myelin Protein Zero Neuropathies in Transgenic Mice

Missense mutations in 22 genes account for one-quarter of Charcot–Marie–Tooth (CMT) hereditary neuropathies. Myelin Protein Zero (MPZ, P0) mutations produce phenotypes ranging from adult demyelinating (CMT1B) to early onset [Déjérine-Sottas syndrome (DSS) or congenital hypomyelination] to predominan...

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Udgivet i:J Neurosci
Main Authors: Wrabetz, Lawrence, D’Antonio, Maurizio, Pennuto, Maria, Dati, Gabriele, Tinelli, Elisa, Fratta, Pietro, Previtali, Stefano, Imperiale, Daniele, Zielasek, Jurgen, Toyka, Klaus, Avila, Robin L., Kirschner, Daniel A., Messing, Albee, Feltri, M. Laura, Quattrini, Angelo
Format: Artigo
Sprog:Inglês
Udgivet: Society for Neuroscience 2006
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Articles
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6674823/
https://ncbi.nlm.nih.gov/pubmed/16495463
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.3819-05.2006
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