A novel mutation in SLC1A3 causes episodic ataxia
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DOI: 10.1038/s10038-017-0365-z
Abstract: Episodic ataxias (EAs) are rare channelopathies characterized by recurrent ataxia and vertigo, having eight subtypes. Mutated genes were found in four of these eight subtypes (EA1, EA2, EA5, and EA6). To date, only four missense… read more here.
Keywords: slc1a3; slc1a3 causes; novel mutation; mutation slc1a3 ... See more keywords