Clinical characteristics of combined cases of spinocerebellar ataxia types 6 and 31
Author:
Publisher
Informa UK Limited
Subject
Cellular and Molecular Neuroscience,Genetics
Link
http://www.tandfonline.com/doi/pdf/10.3109/01677063.2015.1054992
Reference22 articles.
1. Clinical characteristics of patients with spinocerebellar ataxias 1, 2, 3 and 6 in the US; a prospective observational study
2. Autosomal dominant cerebellar ataxia type III: a review of the phenotypic and genotypic characteristics
3. THE CLINICAL FEATURES AND CLASSIFICATION OF THE LATE ONSET AUTOSOMAL DOMINANT CEREBELLAR ATAXIAS
4. Japanese Families with Autosomal Dominant Pure Cerebellar Ataxia Map to Chromosome 19p13.1-p13.2 and Are Strongly Associated with Mild CAG Expansions in the Spinocerebellar Ataxia Type 6 Gene in Chromosome 19p13.1
5. Abundant expression and cytoplasmic aggregations of alpha1A voltage-dependent calcium channel protein associated with neurodegeneration in spinocerebellar ataxia type 6
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 type 31: A clinical and radiological literature review;Journal of the Neurological Sciences;2023-01
2. Neurodegenerative diseases: From the bench to the clinic;Journal of Neurogenetics;2015-07-03
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