A gene for episodic ataxia/myokymia maps to chromosome 12p13.

Episodic ataxia (EA) is a rare, familial disorder producing attacks of generalized ataxia, with normal or near-normal neurological function between attacks. Families with autosomal dominant EA represent at least two distinct clinical syndromes. One clinical type of EA (MIM 160120) includes individua...

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Main Authors: Litt, M., Kramer, P., Browne, D., Gancher, S., Brunt, E. R., Root, D., Phromchotikul, T., Dubay, C. J., Nutt, J.
格式: Artigo
語言:Inglês
出版: 1994
主題:
Research Article
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC1918305/
https://ncbi.nlm.nih.gov/pubmed/7942848
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