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Q30040543-19413A95-2DEC-429E-B294-6E6E0D0EB3C8
Q30040543-19413A95-2DEC-429E-B294-6E6E0D0EB3C8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30040543-19413A95-2DEC-429E-B294-6E6E0D0EB3C8
PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome
P2860
Q30040543-19413A95-2DEC-429E-B294-6E6E0D0EB3C8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30040543-19413A95-2DEC-429E-B294-6E6E0D0EB3C8
rank
NormalRank
type
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wasDerivedFrom
659daa87e036096e564b99755d6c9058d5c1ae4b
P2860
MTHFR C677T polymorphism and risk of congenital heart defects: evidence from 29 case-control and TDT studies.