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Q33847202-B20C3280-E3F7-4BD3-B519-CDE460574E7F
Q33847202-B20C3280-E3F7-4BD3-B519-CDE460574E7F
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Statement
http://www.wikidata.org/entity/statement/Q33847202-B20C3280-E3F7-4BD3-B519-CDE460574E7F
Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes.
P2860
Q33847202-B20C3280-E3F7-4BD3-B519-CDE460574E7F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33847202-B20C3280-E3F7-4BD3-B519-CDE460574E7F
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wasDerivedFrom
bc0f280ba800b72821ce1e91dfd67bd19f3a017a
P2860
A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy