Point mutations in murine Nkx2-5 phenocopy human congenital heart disease and induce pathogenic Wnt signaling-Reference-Cited by-同舟云学术

Point mutations in murine Nkx2-5 phenocopy human congenital heart disease and induce pathogenic Wnt signaling

Published:2017-03-23 Issue:6 Volume:2 Page:
ISSN:2379-3708
Container-title:JCI Insight
language:en
Short-container-title:

Author:

Furtado Milena B.,Wilmanns Julia C.,Chandran Anjana,Perera Joelle,Hon Olivia,Biben Christine,Willow Taylor J.,Nim Hieu T.,Kaur Gurpreet,Simonds Stephanie,Wu Qizhu,Willians David,Salimova Ekaterina,Plachta Nicolas,Denegre James M.,Murray Stephen A.,Fatkin Diane,Cowley Michael,Pearson James T.,Kaye David,Ramialison Mirana,Harvey Richard P.,Rosenthal Nadia A.,Costa Mauro W.

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference70 articles.

1. Genetic factors in non-syndromic congenital heart malformations

2. Genetics of Congenital Heart Disease

3. The changing epidemiology of congenital heart disease

4. Congenital Heart Disease in Adults

5. Genetic Origins of Pediatric Heart Disease

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