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pubmed-article:10371528pubmed:abstractTextTo characterize the nature of CACNA1A mutations in episodic ataxia type 2 (EA2), to search for mutations in sporadic cases, and to delineate better the clinical spectrum.lld:pubmed
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pubmed-article:10371528pubmed:articleTitleHigh prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2.lld:pubmed
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