Novel Point Mutations in the NKX2.5 Gene in Pediatric Patients with Non-Familial Congenital Heart Disease

Mutation analysis of the NKX2.5 gene in Iranian pediatric patients with congenital hypothyroidism

(2017) Mehri Khatami et al.   JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM

Genetics of Congenital Heart Disease: Past and Present

(2016) Iolanda Muntean et al.   BIOCHEMICAL GENETICS

Genetic variations of NKX2-5 in sporadic atrial septal defect and ventricular septal defect in Chinese Yunnan population

(2016) Yu Cao et al.   GENE

Existence of mutations in the homeodomain-encoding region of NKX2.5 gene in Iranian patients with tetralogy of Fallot

(2016) Majid Kheirollahi et al.   Journal of Research in Medical Sciences

Cardiac Phenotype and Long-Term Follow-Up of Patients With Mutations in NKX2-5 Gene

(2016) Philippe Maury et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Genetics of Congenital Heart Defects: The NKX2-5 Gene, a Key Player

(2016) Ill-Min Chung et al.   Genes

Investigation ofNKX2.5Gene Mutations in Congenital Heart Defects in an Indian Population

(2015) Sarada Ketharnathan et al.   Genetic Testing and Molecular Biomarkers

Two novel and functional DNA sequence variants within an upstream enhancer of the human NKX2-5 gene in ventricular septal defects

(2013) Wenhui Huang et al.   GENE

Transcriptional Defect of an Inherited NKX2-5 Haplotype Comprising a SNP, a Nonsynonymous and a Synonymous Mutation, Associated with Human Congenital Heart Disease

(2013) Stella Marie Reamon-Buettner et al.   PLoS One

Combined Mutation Screening of NKX2-5, GATA4, and TBX5 in Congenital Heart Disease: Multiple Heterozygosity and Novel Mutations

(2011) Javier T. Granados-Riveron et al.   Congenital Heart Disease

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

(2010) B Stallmeyer et al.   CLINICAL GENETICS

Molecular mechanisms of congenital heart disease

(2009) Huang Jing-bin et al.   CARDIOVASCULAR PATHOLOGY

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

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

Screening NXK2.5 Mutation in a Sample of 230 Han Chinese Children with Congenital Heart Diseases

(2009) Weimin Zhang et al.   Genetic Testing and Molecular Biomarkers

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

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