Recurrent Episodes of Stroke-Like Symptoms in a Patient with Charcot-Marie-Tooth Neuropathy X Type 1

Charcot-Marie-Tooth disease (CMT), also known as hereditary motor sensory neuropathy, is a heterogeneous group of disorders best known for causing inherited forms of peripheral neuropathy. The X-linked form, CMTX1, is caused by mutations in the gap junction protein beta 1 (GJB1) gene, expressed both...

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Detalles Bibliográficos
Autores principales: Wu, Ning, Said, Sarita, Sabat, Shyamsunder, Wicklund, Matthew, Stahl, Mark C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2015
Materias:
Published online: December, 2015
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4777946/
https://www.ncbi.nlm.nih.gov/pubmed/26955336
http://dx.doi.org/10.1159/000442410

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4777946/
https://www.ncbi.nlm.nih.gov/pubmed/26955336
http://dx.doi.org/10.1159/000442410

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