NKX2.5 mutations and congenital heart disease: Is it a marker of cardiac anomalies?

International Journal of Cardiology

Volumn 147, Issue 3, 2011, Pages

  Balci, Mustafa M ^a   Akdemir, Ramazan ^a  

^a Diskapi Education and Research Hospital   (Turkey)

Author keywords

Congenital heart disease; Genetic counseling; NKX 2.5 mutation

Indexed keywords

BONE MORPHOGENETIC PROTEIN 4; TRANSCRIPTION FACTOR GATA 4; TRANSCRIPTION FACTOR NKX2.5; TRANSCRIPTION FACTOR TBX5;

ARTICLE; CONGENITAL HEART DISEASE; CRELD1 GENE; DISEASE MARKER; FALLOT TETRALOGY; GENE; GENE FREQUENCY; GENE IDENTIFICATION; GENETIC ASSOCIATION; GENETIC MARKER; GENOTYPE PHENOTYPE CORRELATION; HEART DEVELOPMENT; HEART SEPTUM DEFECT; HETEROZYGOSITY; HUMAN; MISSENSE MUTATION; MUTATIONAL ANALYSIS; NKX2.5 GENE; NONSENSE MUTATION; PRIORITY JOURNAL; TRANSCRIPTION REGULATION;

HAND DEFORMITIES, CONGENITAL; HOMEODOMAIN PROTEINS; HUMANS; POINT MUTATION; TRANSCRIPTION FACTORS;

EID: 79952483916     PISSN: 01675273     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ijcard.2009.01.024     Document Type: Article

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