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Q35078014-872A1AA0-F409-40F0-8E76-14F69C095EE1
Q35078014-872A1AA0-F409-40F0-8E76-14F69C095EE1
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http://www.wikidata.org/entity/statement/Q35078014-872A1AA0-F409-40F0-8E76-14F69C095EE1
Transcriptional defect of an inherited NKX2-5 haplotype comprising a SNP, a nonsynonymous and a synonymous mutation, associated with human congenital heart disease.
P2860
Q35078014-872A1AA0-F409-40F0-8E76-14F69C095EE1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35078014-872A1AA0-F409-40F0-8E76-14F69C095EE1
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wasDerivedFrom
72cc37b9967be8d585b003231c948488f0dea62e
P2860
A functional genetic study identifies HAND1 mutations in septation defects of the human heart