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bn:04726809n
Noun Concept
JA
No term available
EN
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 Wikidata
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Sources
IS A
遺伝子疾患
側頭葉てんか
GENETIC ASSOCIATION
リーリン

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