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Q58589688-B7F80074-A270-43A9-84C3-6E91B1E938A5
Q58589688-B7F80074-A270-43A9-84C3-6E91B1E938A5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58589688-B7F80074-A270-43A9-84C3-6E91B1E938A5
Origin and age of the causative mutations in KLC2, IMPA1, MED25 and WNT7A unravelled through Brazilian admixed populations
P2860
Q58589688-B7F80074-A270-43A9-84C3-6E91B1E938A5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58589688-B7F80074-A270-43A9-84C3-6E91B1E938A5
rank
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type
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Statement
wasDerivedFrom
7491c607efdc0d5103592df28e49455d304d2996
P2860
A homozygous loss-of-function mutation in inositol monophosphatase 1 (IMPA1) causes severe intellectual disability.