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Q52910100-26015F06-17DA-44F5-ABD2-CF8E78A16599
Q52910100-26015F06-17DA-44F5-ABD2-CF8E78A16599
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52910100-26015F06-17DA-44F5-ABD2-CF8E78A16599
Novel loss-of-function variants in DIAPH1 associated with syndromic microcephaly, blindness, and early onset seizures.
P2860
Q52910100-26015F06-17DA-44F5-ABD2-CF8E78A16599
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52910100-26015F06-17DA-44F5-ABD2-CF8E78A16599
rank
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type
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Statement
wasDerivedFrom
70958d88414ff69611e4835de5481bb9da552d90
P2860
Homozygous loss of DIAPH1 is a novel cause of microcephaly in humans