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Q41126903-0405F7A1-2155-471A-A4DB-82C418AD64E5
Q41126903-0405F7A1-2155-471A-A4DB-82C418AD64E5
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Statement
http://www.wikidata.org/entity/statement/Q41126903-0405F7A1-2155-471A-A4DB-82C418AD64E5
A TBX5 3'UTR variant increases the risk of congenital heart disease in the Han Chinese population.
P2860
Q41126903-0405F7A1-2155-471A-A4DB-82C418AD64E5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41126903-0405F7A1-2155-471A-A4DB-82C418AD64E5
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Statement
wasDerivedFrom
8c88fedffeaa373808adcc664e708ff13e1d52e7
P2860
Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.