Spinocerebellar Ataxia Type 13 is an Uncommon SCA Subtype in the Chinese Han Population
Author:
Publisher
Informa UK Limited
Subject
General Medicine,General Neuroscience
Link
http://www.tandfonline.com/doi/pdf/10.3109/00207454.2013.763254
Reference25 articles.
1. Spectrin mutations cause spinocerebellar ataxia type 5
2. Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11
3. Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypes
4. Spinocerebellar Ataxia Type 14 Caused by a Mutation in Protein Kinase C γ
5. A Mutation in the Fibroblast Growth Factor 14 Gene Is Associated with Autosomal Dominant Cerebral Ataxia
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Spinocerebellar Ataxia Types 13, 14, 15, and 16☆;Reference Module in Neuroscience and Biobehavioral Psychology;2017
2. Functional Analysis Helps to Define KCNC3 Mutational Spectrum in Dutch Ataxia Cases;PLOS ONE;2015-03-10
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