toIPA
Home
Blog
Category
Familial temporal lobe epilepsy 7
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
Pronunciation
/fəˈmɪljəl ˈtɛmpərəl ləʊb ˈɛpɪlɛpsi 7/
/fəˈmɪljəl ˈtɛmpərəl loʊb ˈɛpəˌlɛpsi 7/
Categories
genetic disease
temporal lobe epilepsy