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Clinical and Genetic Profiles in Chinese Patients with Huntington’s Disease: A Ten-year Multicenter Study in China

Huntington’s disease (HD) is an autosomal dominant inherited neurodegenerative disorder caused by CAG triplet repeats expansion in exon 1 of the Huntingtin gene (HTT). In China, HD is considered to have a low prevalence. The goal of this study was to describe the clinical characteristic and genetic...

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Detalles Bibliográficos
Autores principales:	Li, Hong-Lei, Li, Xiao-Yan, Dong, Yi, Zhang, Yan-Bin, Cheng, Hong-Rong, Gan, Shi-Rui, Liu, Zhi-Jun, Ni, Wang, Burgunder, Jean-Marc, Yang, X. William, Wu, Zhi-Ying
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	JKL International LLC 2019
Materias:	Orginal Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6764736/ https://www.ncbi.nlm.nih.gov/pubmed/31595198 http://dx.doi.org/10.14336/AD.2018.0911

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