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bn:15670519n
Noun Concept
EL
No term available
EN
Norman–Roberts syndrome is a rare form of microlissencephaly caused by a mutation in the RELN gene. Wikipedia
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Sources
IS A
σπάνια πάθηση
γενετική διαταραχή
lissencephaly
EN
autosomal recessive disease
EN
microlissencephaly
GENETIC ASSOCIATION
ρεελίνη
HEALTH SPECIALTY
Ιατρική γενετική

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