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Molecular Mechanisms of Inherited Demyelinating Neuropathies

The past 15 years have witnessed the identification of more than 25 genes responsible for inherited neuropathies in humans, many associated with primary alterations of the myelin sheath. A remarkable body of work in patients, as well as animal and cellular models, has defined the clinical and molecu...

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Detalhes bibliográficos
Main Authors: SCHERER, STEVEN S., WRABETZ, LAWRENCE
Formato: Artigo
Idioma:Inglês
Publicado em: 2008
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2570024/
https://ncbi.nlm.nih.gov/pubmed/18803325
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/glia.20751
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