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bn:15670519n
Noun Concept
JA
No term available
EN
Norman–Roberts syndrome is a rare form of microlissencephaly caused by a mutation in the RELN gene. Wikipedia
Relations
Sources
IS A
希少疾患
遺伝子疾患
滑脳症
EN
autosomal recessive disease
EN
microlissencephaly
GENETIC ASSOCIATION
リーリン
HEALTH SPECIALTY
遺伝医学

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