Clinical Diversity of SCN4A-Mutation-Associated Skeletal Muscle Sodium Channelopathy

BACKGROUND AND PURPOSE: Mutations of the skeletal muscle sodium channel gene SCN4A, which is located on chromosome 17q23-25, are associated with various neuromuscular disorders that are labeled collectively as skeletal muscle sodium channelopathy. These disorders include hyperkalemic periodic paraly...

Descripción completa

Detalles Bibliográficos
Autores principales: Lee, Sang-Chan, Kim, Hyang-Sook, Park, Yeong-Eun, Choi, Young-Chul, Park, Kyu-Hyun, Kim, Dae-Seong
Formato: Texto
Lenguaje:English
Publicado: Korean Neurological Association 2009
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2806541/
https://www.ncbi.nlm.nih.gov/pubmed/20076800
http://dx.doi.org/10.3988/jcn.2009.5.4.186

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2806541/
https://www.ncbi.nlm.nih.gov/pubmed/20076800
http://dx.doi.org/10.3988/jcn.2009.5.4.186

Ejemplares similares