Familial temporal lobe epilepsy 5

MONDO:0013741

A temporal lobe epilepsy that has material basis in heterozygous mutation in the CPA6 gene on chromosome 8q13.

Also known as: ETL5, epilepsy, familial temporal lobe, type 5, familial temporal lobe epilepsy type 5, epilepsy, familial temporal lobe, 5

9 clinical trials for this condition and its sub-types.

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