A temporal lobe epilepsy that has material basis in heterozygous mutation in the CPA6 gene on chromosome 8q13.
Comprehensive, easy-to-understand information about this condition
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familial temporal lobe epilepsy 2
MONDO:0011965
familial temporal lobe epilepsy 4
MONDO:0012706
familial temporal lobe epilepsy 6
MONDO:0014308
familial temporal lobe epilepsy 7
MONDO:0014639
familial temporal lobe epilepsy 8
MONDO:0014650
epilepsy, familial temporal lobe, 1
MONDO:0700090