Familial temporal lobe epilepsy 7
MONDO:0014639A temporal lobe epilepsy characterized by autosomal dominant inheritance of focal seizures with prominent auditory symptoms and that has material basis in heterozygous mutation in the RELN gene on chromosome 7q22.
Also known as: ETL7, epilepsy, familial temporal lobe, type 7, familial temporal lobe epilepsy type 7, epilepsy, familial temporal lobe, 7
10 clinical trials for this condition and its sub-types, 0 tagged with Familial temporal lobe epilepsy 7 itself.
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