Novel and Highly Lethal NKX2.5 Missense Mutation in a Family With Sudden Death and Ventricular Arrhythmia

Functional Characterization of a Novel Mutation in NKX2-5 Associated With Congenital Heart Disease and Adult-Onset Cardiomyopathy

(2013) Mauro W. Costa et al.   Circulation-Cardiovascular Genetics

Prevalence and spectrum of Nkx2.5 mutations associated with idiopathic atrial fibrillation

(2013) WH Xie et al.   Clinics

Evolutionary conservation of Nkx2.5 autoregulation in the second heart field

(2012) Christopher D. Clark et al.   DEVELOPMENTAL BIOLOGY

A de novo mutation in NKX2.5 associated with atrial septal defects, ventricular noncompaction, syncope and sudden death

(2010) Ping Ouyang et al.   CLINICA CHIMICA ACTA

Mutational spectrum in the cardiac transcription factor gene NKX2.5 (CSX) associated with congenital heart disease

(2010) B Stallmeyer et al.   CLINICAL GENETICS

Genetic Origins of Pediatric Heart Disease

(2009) D. Woodrow Benson   PEDIATRIC CARDIOLOGY

Clinical and Molecular Analysis of Thyroid Hypoplasia: A Population-Based Approach in Southern Brazil

(2008) Helton E. Ramos et al.   THYROID