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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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Библиографические подробности
Главные авторы: SCHERER, STEVEN S., WRABETZ, LAWRENCE
Формат: Artigo
Язык:Inglês
Опубликовано: 2008
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Online-ссылка: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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