Familial Atrial Septal Defect and Sudden Cardiac Death: Identification of a NovelNKX2-5Mutation and a Review of the Literature

Atrial fibrillation and stroke in adult patients with atrial septal defect and the long-term effect of closure

(2015) C Nyboe et al.   HEART

NKX2-5 Mutations in an Inbred Consanguineous Population: Genetic and Phenotypic Diversity

(2015) Ossama K. Abou Hassan et al.   Scientific Reports

Risk of Pneumonia in Adults With Closed Versus Unclosed Atrial Septal Defect (from a Nationwide Cohort Study)

(2014) Camilla Nyboe et al.   AMERICAN JOURNAL OF CARDIOLOGY

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

(2014) Jennifer L. Perera et al.   PEDIATRIC CARDIOLOGY

Prevalence of congenital heart disease at live birth: an accurate assessment by echocardiographic screening

(2013) Qu-ming Zhao et al.   ACTA PAEDIATRICA

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

Controversies in the definition and management of insignificant left-to-right shunts

(2013) Massimiliano Cantinotti et al.   HEART

Genetic Analysis of Essential Cardiac Transcription Factors in 256 Patients With Non-Syndromic Congenital Heart Defects

(2012) Kazuki Kodo et al.   CIRCULATION JOURNAL

Normal and abnormal development of the cardiac conduction system; implications for conduction and rhythm disorders in the child and adult

(2012) Monique R.M. Jongbloed et al.   DIFFERENTIATION

Organogenesis of the vertebrate heart

(2012) Lucile Miquerol et al.   Wiley Interdisciplinary Reviews-Developmental Biology

Birth Prevalence of Congenital Heart Disease Worldwide

(2011) Denise van der Linde et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

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

Mutations of the GATA4 and NKX2.5 genes in Chinese pediatric patients with non-familial congenital heart disease

(2010) Ting Peng et al.   GENETICA

Novel NKX2-5 Mutations in Patients With Familial Atrial Septal Defects

(2010) Xing-Yuan Liu et al.   PEDIATRIC CARDIOLOGY

Molecular analysis ofPRKAG2,LAMP2, andNKX2-5genes in a cohort of 125 patients with accessory atrioventricular connection

(2009) Giorgia Esposito et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Mutations in the NKX2-5 gene in patients with stroke and patent foramen ovale

(2009) Robert Belvís et al.   CLINICAL NEUROLOGY AND NEUROSURGERY

NKX2.5 mutations in patients with non-syndromic congenital heart disease

(2008) Luciana Gioli-Pereira et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY