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Q36616304-90063185-21D7-4F7B-AAAF-01D0B881C9E4
Q36616304-90063185-21D7-4F7B-AAAF-01D0B881C9E4
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Statement
http://www.wikidata.org/entity/statement/Q36616304-90063185-21D7-4F7B-AAAF-01D0B881C9E4
Molecular subtyping and improved treatment of neurodevelopmental disease.
P2860
Q36616304-90063185-21D7-4F7B-AAAF-01D0B881C9E4
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36616304-90063185-21D7-4F7B-AAAF-01D0B881C9E4
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wasDerivedFrom
9288b3ef1af6e4d3234f55f00cdcb9f5c9aa3265
P2860
Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndrome.