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

International Journal of Cardiology

Volumn 138, Issue 3, 2010, Pages 261-265

  Gioli Pereira, Luciana ^a   Pereira, Alexandre Costa ^a   Mesquita, Sônia M ^a   Xavier Neto, José ^a   Lopes, Antônio Augusto ^a   Krieger, José Eduardo ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

Congenital heart disease; Human; Mutation; NKX2.5

Indexed keywords

ALANINE; ARGININE; CYSTEINE; PROLINE; TRANSCRIPTION FACTOR NKX2.5;

AORTA COARCTATION; AORTA SUBVALVULAR STENOSIS; AORTA VALVE STENOSIS; ARTICLE; ATRIOVENTRICULAR BLOCK; BLALOCK TAUSSIG SHUNT; CHILD; CONGENITAL HEART DISEASE; DENATURING HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; DNA SEQUENCE; EBSTEIN ANOMALY; FALLOT TETRALOGY; GENE AMPLIFICATION; GENE MUTATION; GENETIC ASSOCIATION; GREAT VESSELS TRANSPOSITION; HEART ATRIUM FIBRILLATION; HEART ATRIUM SEPTUM DEFECT; HEART INJURY; HEART RIGHT VENTRICLE DOUBLE OUTLET; HEART SEPTUM DEFECT; HEART VENTRICLE SEPTUM DEFECT; HUMAN; INFANT; MAJOR CLINICAL STUDY; MITRAL VALVE REGURGITATION; MUTATION RATE; MUTATIONAL ANALYSIS; PATENT DUCTUS ARTERIOSUS; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; PRIORITY JOURNAL; PROSPECTIVE STUDY; PULMONARY HYPERTENSION; PULMONARY VALVE STENOSIS; TRICUSPID VALVE REGURGITATION; WOLFF PARKINSON WHITE SYNDROME;

AMINO ACID SEQUENCE; DNA MUTATIONAL ANALYSIS; DUCTUS ARTERIOSUS, PATENT; EBSTEIN ANOMALY; HAND DEFORMITIES, CONGENITAL; HEART SEPTAL DEFECTS; HOMEODOMAIN PROTEINS; HUMANS; POINT MUTATION; POLYMERASE CHAIN REACTION; TETRALOGY OF FALLOT; TRANSCRIPTION FACTORS;

EID: 74449089010     PISSN: 01675273     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ijcard.2008.08.035     Document Type: Article

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