PhD Hannu Somer MD

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Sirs: Episodic ataxia type 2 (EA-2) is a rare neurological disease characterized by episodes of vertigo, ataxia, nystagmus, nausea, vomiting, fatigue, and often migraine. EA-2 is inherited as an autosomal dominant trait of the CACNA1A gene mutations on chromosome 19p13. CACNA1A encodes the alpha1A-subunit of a voltage dependent P/Q-type calcium channel that(More)
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