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CACNA1A activates Episodic familial ataxia type 2. 1 / 1

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"Episodic familial ataxia type 2 is caused by mutations in the gene CACNA1A, in chromosome 19p, that codifies part of a calcium channel."

9859670

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IndraLab

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CACNA1A activates Episodic familial ataxia type 2. 1 / 1

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