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Q36339532-97324CDD-268B-451D-A99A-08A799A08B6D
Q36339532-97324CDD-268B-451D-A99A-08A799A08B6D
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http://www.wikidata.org/entity/statement/Q36339532-97324CDD-268B-451D-A99A-08A799A08B6D
Genetic abnormalities in bicuspid aortic valve root phenotype: preliminary results†.
P2860
Q36339532-97324CDD-268B-451D-A99A-08A799A08B6D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36339532-97324CDD-268B-451D-A99A-08A799A08B6D
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wasDerivedFrom
7ee26e67ad76635c9870e3a97a86f487477f9113
P2860
Transcriptional defect of an inherited NKX2-5 haplotype comprising a SNP, a nonsynonymous and a synonymous mutation, associated with human congenital heart disease.