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Q30389650-C4DFB634-9890-4B83-9D60-7D2FB0889D6F
Q30389650-C4DFB634-9890-4B83-9D60-7D2FB0889D6F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30389650-C4DFB634-9890-4B83-9D60-7D2FB0889D6F
Auditory deficits of Kcna1 deletion are similar to those of a monaural hearing impairment.
P2860
Q30389650-C4DFB634-9890-4B83-9D60-7D2FB0889D6F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30389650-C4DFB634-9890-4B83-9D60-7D2FB0889D6F
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Statement
wasDerivedFrom
e1d82e14f81cf44432cb8af468a03686ae5e6c14
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