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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Publicat a:Biomed Res Int
Autors principals: Mai, Phuong-Thao, Le, Dong-Truc, Nguyen, Tan-Trung, Le Gia, Hoang-Linh, Nguyen Le, Trung-Hieu, Le, Minh, Do, Duc-Minh
Format: Artigo
Idioma:Inglês
Publicat: Hindawi 2019
Matèries:
Research Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6507255/
https://ncbi.nlm.nih.gov/pubmed/31179332
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2019/7132494
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars