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migraine, familial hemiplegic
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Long-term depression
Homo sapiens (human)
one gene
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CACNA1A
A new beta subtype-specific interaction in alpha1A subunit controls P/Q-type Ca2+ channel activation
Mutation analysis of the CACNA1A calcium channel subunit gene in 27 patients with sporadic hemiplegic migraine
International Union of Pharmacology. XLVIII. Nomenclature and structure-function relationships of voltage-gated calcium channels
ATP1A2
A novel mutation in the ATP1A2 gene causes alternating hemiplegia of childhood
SCN1A
Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy
Interaction of muscle and brain sodium channels with multiple members of the syntrophin family of dystrophin-associated proteins
Ion channels and epilepsy
Cancer Gene Census
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