Sequencing of Charcot-Marie-Tooth disease genes in a toxic polyneuropathy

OBJECTIVE: Mutations in Charcot-Marie-Tooth disease (CMT) genes are the cause of rare familial forms of polyneuropathy. Whether allelic variability in CMT genes is also associated with common forms of polyneuropathy—considered “acquired” in medical parlance—is unknown. Chemotherapy induced periphera...

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Опубликовано в: :Ann Neurol
Главные авторы: Beutler, Andreas S., Kulkarni, Amit A., Kanwar, Rahul, Klein, Christopher J., Therneau, Terry M., Qin, Rui, Banck, Michaela S., Boora, Ganesh K., Ruddy, Kathryn J., Wu, Yanhong, Smalley, Regenia L., Cunningham, Julie M., Le-Lindqwister, Nguyet Anh, Beyerlein, Peter, Schroth, Gary P., Windebank, Anthony J., Züchner, Stephan, Loprinzi, Charles L.
Формат: Artigo
Язык:Inglês
Опубликовано: 2014
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Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC4388308/
https://ncbi.nlm.nih.gov/pubmed/25164601
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ana.24265
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