Spinocerebellar ataxia type 6 and episodic ataxia type 2 in a Korean family.

Spinocerebellar ataxia type 6 (SCA6), episodic ataxia type 2 (EA2) and familial hemiplegic migraine (FHM) have been known as allelic disorders, which are caused by the alteration of the alpha1A voltage-dependent calcium channel subunit. Expansions of the CAG repeat in the CACNA1A gene on the short a...

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Main Authors: Koh, S. H., Kim, H. T., Kim, S. H., Lee, G. Y., Kim, J., Kim, M. H.
Formáid: Artigo
Teanga:Inglês
Foilsithe: Korean Academy of Medical Sciences 2001
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Research Article
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3054805/
https://ncbi.nlm.nih.gov/pubmed/11748369
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