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Q58706422-9C0E3948-6D70-4572-8BE9-80A1D5EAFFDC
Q58706422-9C0E3948-6D70-4572-8BE9-80A1D5EAFFDC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58706422-9C0E3948-6D70-4572-8BE9-80A1D5EAFFDC
A loss-of-function mutation p.T52S in RIPPLY3 is a potential predisposing genetic risk factor for Chinese Han conotruncal heart defect patients without the 22q11.2 deletion/duplication
P2860
Q58706422-9C0E3948-6D70-4572-8BE9-80A1D5EAFFDC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58706422-9C0E3948-6D70-4572-8BE9-80A1D5EAFFDC
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type
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Statement
wasDerivedFrom
746d283ea3a0e4ecc6ced9973301a63916d34912
P2860
Genotype and cardiovascular phenotype correlations with TBX1 in 1,022 velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients.