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
Transcriptional factors in calcium mishandling and atrial fibrillation development.
Dai W et al.
Pflugers Archiv : European Journal of Physiology, 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
Mutational spectrum of the NKX2-5 gene in patients with lone atrial fibrillation.
Yu H et al.
International Journal of Medical Sciences, 2014
Prevalence and spectrum of Nkx2.5 mutations associated with idiopathic atrial fibrillation.
Xie WH et al.
Clinics (sao Paulo, Brazil), 2013
Select a paper to view details