Generation of induced pluripotent stem cell line (ZZUi0018-A ) from a patient with spinocerebellar ataxia type 6

Spinocerebellar ataxia type 6 (SCA6) is an autosomal dominant hereditary disease caused by repeated CAG amplification in the CACNA1A gene. There is no specific treatment for SCA6, and the currently administered treatment is mainly symptomatic. The fibroblasts from a patient with SCA6 were successful...

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Bibliographic Details
Main Authors: Ting Yang, Jie Qin, Qi Zhang, Huifang Sun, Zhuoya Wang, Jing yang, Han liu, Chan Zhang, Shoutao Zhang, Jin Zhang, Yanlin Wang, Yuming Xu
Format: Article
Language:English
Published: Elsevier 2020-04-01
Series:Stem Cell Research
Online Access:http://www.sciencedirect.com/science/article/pii/S1873506120300817