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Q38920317-2B8AE06B-55B4-47BE-88DB-B59EED78EA8A
Q38920317-2B8AE06B-55B4-47BE-88DB-B59EED78EA8A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38920317-2B8AE06B-55B4-47BE-88DB-B59EED78EA8A
An update on the molecular diagnosis of congenital heart disease: focus on loss-of-function mutations.
P2860
Q38920317-2B8AE06B-55B4-47BE-88DB-B59EED78EA8A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38920317-2B8AE06B-55B4-47BE-88DB-B59EED78EA8A
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Statement
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e3199e59f19deaf6f9429ffab714482e0340847e
P2860
Rare variants in NR2F2 cause congenital heart defects in humans.