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Q28073446-8E7955CA-B595-46A8-AB7B-E9BE244F3DE2
Q28073446-8E7955CA-B595-46A8-AB7B-E9BE244F3DE2
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Statement
http://www.wikidata.org/entity/statement/Q28073446-8E7955CA-B595-46A8-AB7B-E9BE244F3DE2
New insights into the generation and role of de novo mutations in health and disease
P2860
Q28073446-8E7955CA-B595-46A8-AB7B-E9BE244F3DE2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28073446-8E7955CA-B595-46A8-AB7B-E9BE244F3DE2
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wasDerivedFrom
f47530d1287ebf721d480be5525b98ce48da45f0
P2860
Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndrome.