Novel GDAP1 Mutation in a Vietnamese Family with Charcot-Marie-Tooth Disease

BACKGROUND: Mutations of GDAP1 gene cause autosomal dominant and autosomal recessive Charcot-Marie-Tooth (CMT) disease and over 80 different mutations have been identified so far. This study analyzed the clinical and genetic characteristics of a Vietnamese CMT family that was affected by a novel GDA...

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Detalles Bibliográficos
Autores principales: Mai, Phuong-Thao, Le, Dong-Truc, Nguyen, Tan-Trung, Le Gia, Hoang-Linh, Nguyen Le, Trung-Hieu, Le, Minh, Do, Duc-Minh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6507255/
https://www.ncbi.nlm.nih.gov/pubmed/31179332
http://dx.doi.org/10.1155/2019/7132494

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6507255/
https://www.ncbi.nlm.nih.gov/pubmed/31179332
http://dx.doi.org/10.1155/2019/7132494

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