Shortened internodal length of dermal myelinated nerve fibres in Charcot–Marie-Tooth disease type 1A

Charcot–Marie-Tooth disease type 1A is the most common inherited neuropathy and is caused by duplication of chromosome 17p11.2 containing the peripheral myelin protein-22 gene. This disease is characterized by uniform slowing of conduction velocities and secondary axonal loss, which are in contrast...

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Detaylı Bibliyografya
Asıl Yazarlar: Saporta, Mario A., Katona, Istvan, Lewis, Richard A., Masse, Stacey, Shy, Michael E., Li, Jun
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Oxford University Press 2009
Konular:
Original Articles
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2800385/
https://ncbi.nlm.nih.gov/pubmed/19923170
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/brain/awp274
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