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Q30040543-18897B50-69F8-4658-A6A7-D101BE564EDC
Q30040543-18897B50-69F8-4658-A6A7-D101BE564EDC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30040543-18897B50-69F8-4658-A6A7-D101BE564EDC
PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome
P2860
Q30040543-18897B50-69F8-4658-A6A7-D101BE564EDC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q30040543-18897B50-69F8-4658-A6A7-D101BE564EDC
rank
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type
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Statement
wasDerivedFrom
659daa87e036096e564b99755d6c9058d5c1ae4b
P2860
Genetic basis of congenital cardiovascular malformations