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Q38920317-202B5D06-1FD9-491D-9893-2A8644F30FFE
Q38920317-202B5D06-1FD9-491D-9893-2A8644F30FFE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38920317-202B5D06-1FD9-491D-9893-2A8644F30FFE
An update on the molecular diagnosis of congenital heart disease: focus on loss-of-function mutations.
P2860
Q38920317-202B5D06-1FD9-491D-9893-2A8644F30FFE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38920317-202B5D06-1FD9-491D-9893-2A8644F30FFE
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wasDerivedFrom
e3199e59f19deaf6f9429ffab714482e0340847e
P2860
PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome