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Q36695120-4C60633A-ABBD-47DA-9F3D-BC4D76B1DF44
Q36695120-4C60633A-ABBD-47DA-9F3D-BC4D76B1DF44
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36695120-4C60633A-ABBD-47DA-9F3D-BC4D76B1DF44
Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndrome.
P2860
Q36695120-4C60633A-ABBD-47DA-9F3D-BC4D76B1DF44
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36695120-4C60633A-ABBD-47DA-9F3D-BC4D76B1DF44
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wasDerivedFrom
3a47e51cd72fa8e7ffa013b1e8583aa97a973008
P2860
De novo mutations revealed by whole-exome sequencing are strongly associated with autism