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Spinocerebellar ataxia type 6 with positional vertigo and acetazolamide responsive episodic ataxia

The SCA6 mutation, a small expansion of a CAG repeat in a calcium channel gene CACNA1A, was identified in three pedigrees. Point mutations in other parts of the gene CACNA1A were excluded and new clinical features of SCA6 reported—namely, central positional nystagmus and episodic ataxia responsive t...

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Bibliografiske detaljer
Main Authors: Jen, J., Yue, Q., Karrim, J., Nelson, S., Baloh, R.
Format: Artigo
Sprog:Inglês
Udgivet: BMJ Group 1998
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2170265/
https://ncbi.nlm.nih.gov/pubmed/9771787
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