Progressive myoclonic epilepsy type 7

MONDO:0014521

Any progressive myoclonic epilepsy in which the cause of the disease is a mutation in the KCNC1 gene.

Also known as: EPM7, KCNC1 progressive myoclonic epilepsy, MEAK, PME type 7, epilepsy, progressive myoclonic type 7, meak, myoclonus epilepsy and ataxia due to potassium channel mutation, progressive myoclonic epilepsy caused by mutation in KCNC1

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