Clinical and Pathological Features of Korean Patients with DNM2-Related Centronuclear Myopathy

BACKGROUND AND PURPOSE: Centronuclear myopathy (CNM) is characterized by the presence of central nuclei within a large number of muscle fibers. Mutations of the dynamin 2 gene (DNM2) are common causes of autosomal dominant or sporadic CNM. The aim of this study was to characterize the clinical and p...

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Detalles Bibliográficos
Autores principales: Park, Young-Eun, Choi, Young-Chul, Bae, Jong-Suk, Lee, Chang-Hoon, Kim, Hyang-Suk, Shin, Jin-Hong, Kim, Dae-Seong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Neurological Association 2014
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3896645/
https://www.ncbi.nlm.nih.gov/pubmed/24465259
http://dx.doi.org/10.3988/jcn.2014.10.1.24

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3896645/
https://www.ncbi.nlm.nih.gov/pubmed/24465259
http://dx.doi.org/10.3988/jcn.2014.10.1.24

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