Infantile Spinocerebellar Ataxia Type 6: Relationship to Episodic Ataxia Type 6
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Developmental Neuroscience,Neurology,Pediatrics, Perinatology, and Child Health
Reference10 articles.
1. Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the α 1 A voltage-dependent calcium channel;Zhuchenko;Nature Genet,1997
2. Clinical and molecular correlations in spinocerebellar ataxia type 6;Sinke;Arch Neurol,2001
3. Molecular features of the CAG repeats of spinocerebellar ataxia 6 (SCA6);Matsuyama;Hum Mol Genet,1997
4. Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the ca2+ channel gene CACNL 1A4;Ophoff;Cell,1996
5. Spinocerebellar ataxia type 6;Schols;J Neurol Neurosurg Psychiatry,1998
Cited by 1 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. Congenital Ataxia, Mental Retardation, and Dyskinesia Associated With a Novel CACNA1A Mutation;Journal of Child Neurology;2010-01-21
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