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KCNC3 activates voltage-gated potassium channel. 2 / 2

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"SCA13 is caused by mutations in the KCNC3 allele encoding the voltage-gated potassium channel KCNC3/Kv3.3."

31666796

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"A rare form of dominantly inherited ataxia, SCA13 is caused by mutations in the KCNC3 gene encoding the voltage gated potassium channel protein, Kv3.3."

19822774

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IndraLab

Statements

KCNC3 activates voltage-gated potassium channel. 2 / 2

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