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Unmasking a Case of Asymptomatic Charcot-Marie-Tooth Disease (CMT1A) With Vincristine

Charcot-Marie-Tooth (CMT) disease is a hereditary demyelinating disease of the peripheral nervous system that results in sensory and motor dysfunction. CMT includes a spectrum of diseases with different types of mutations in the genes encoding myelin protein, resulting in a variety of dysfunctions i...

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Detaylı Bibliyografya
Yayımlandı:J Investig Med High Impact Case Rep
Asıl Yazarlar: Jariwal, Roopam, Shoua, Basel, Sabetian, Katayoun, Natarajan, Piruthiviraj, Cobos, Everardo
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: SAGE Publications 2018
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5833168/
https://ncbi.nlm.nih.gov/pubmed/29511693
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/2324709618758349
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