Oligogenic inheritance of a human heart disease involving a genetic modifier

scientific article published on 30 May 2019

Oligogenic inheritance of a human heart disease involving a genetic modifier is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1126/SCIENCE.AAT5056
P932PMC publication ID6557373
P698PubMed publication ID31147515

P50authorRyan SamarakoonQ59750816
Stacia K WymanQ89998191
Casey A GiffordQ92418795
Tarja De SoysaQ92418797
Yen Kim BuiQ92418801
Deepak SrivastavaQ92418805
P2093author name stringPing Zhou
Yu Huang
Kathryn N Ivey
Sanjeev S Ranade
Kimberly R Cordes Metzler
Philip Ursell
Aryé Elfenbein
Hazel T Salunga
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Transcriptional defect of an inherited NKX2-5 haplotype comprising a SNP, a nonsynonymous and a synonymous mutation, associated with human congenital heart diseaseQ35078014
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Endothelial deletion of Ino80 disrupts coronary angiogenesis and causes congenital heart diseaseQ48162975
P433issue6443
P407language of work or nameEnglishQ1860
P921main subjectheart diseaseQ190805
P304page(s)865-870
P577publication date2019-05-30
P1433published inScienceQ192864
P1476titleOligogenic inheritance of a human heart disease involving a genetic modifier
P478volume364

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