Transcriptional Defect of an Inherited NKX2-5 Haplotype Comprising a SNP, a Nonsynonymous and a Synonymous Mutation, Associated with Human Congenital Heart Disease-Reference-Cited by-同舟云学术

Transcriptional Defect of an Inherited NKX2-5 Haplotype Comprising a SNP, a Nonsynonymous and a Synonymous Mutation, Associated with Human Congenital Heart Disease

Published:2013-12-20 Issue:12 Volume:8 Page:e83295
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Reamon-Buettner Stella Marie,Sattlegger Evelyn,Ciribilli Yari,Inga Alberto,Wessel Armin,Borlak Jürgen

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference25 articles.

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4. Genetic basis for congenital heart defects: Current knowledge: A scientific statement from the american heart association congenital cardiac defects committee, council on cardiovascular disease in the young: Endorsed by the american academy of pediatrics;ME Pierpont;Circulation,2007

5. Noninherited risk factors and congenital cardiovascular defects: Current knowledge: A scientific statement from the american heart association council on cardiovascular disease in the young: Endorsed by the american academy of pediatrics;KJ Jenkins;Circulation,2007

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4. Functional analysis of novel genetic variants of NKX2 ‐5 associated with nonsyndromic congenital heart disease;American Journal of Medical Genetics Part A;2021-07-02

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