Associated Papers
Functional analysis of novel genetic variants of NKX2-5 associated with nonsyndromic congenital heart disease.
Dixit R et al.
American Journal of Medical Genetics. Part A, 2021
An update on genetic variants of the NKX2-5.
Kolomenski JE et al.
Human Mutation, 2020
A comprehensive in silico analysis, distribution and frequency of human Nkx2-5 mutations; A critical gene in congenital heart disease.
Kalayinia S et al.
Journal of Cardiovascular and Thoracic Research, 2019
NKX2-5 mutations in an inbred consanguineous population: genetic and phenotypic diversity.
Abou Hassan OK et al.
Scientific Reports, 2015
25742962 (PubMed )
Supplement: srep08848-s1.docx
Insights into the genetic structure of congenital heart disease from human and murine studies on monogenic disorders.
Prendiville T et al.
Cold Spring Harbor Perspectives in Medicine, 2014
Novel NKX2-5 mutations responsible for congenital heart disease.
Wang J et al.
Genetics and Molecular Research : Gmr, 2011
[Novel NKX2-5 mutations identified in patients with congenital ventricular septal defects].
Liu XY et al.
Zhonghua Yi Xue Za Zhi, 2009
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