Molecular basis of AV block and cardiac malformations

Cardiovascular Research

Volumn 64, Issue 1, 2004, Pages 1-2

  Mittmann, Clemens ^a  

^a Fed Inst Drugs and Med Devices   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

HOMEODOMAIN PROTEIN; T BOX TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR GATA 4; TRANSCRIPTION FACTOR NKX2.5; UNCLASSIFIED DRUG;

ATRIOVENTRICULAR BLOCK; CHROMOSOME DELETION; CONGENITAL HEART MALFORMATION; DISEASE ASSOCIATION; EDITORIAL; FALLOT TETRALOGY; GENE LOCUS; GENE MUTATION; GENETIC CODE; GENETIC DISORDER; GENOTYPE; HEART SEPTUM DEFECT; HOLT ORAM SYNDROME; HUMAN; LIMB MALFORMATION; PHENOTYPE; PRIORITY JOURNAL; TRISOMY 21;

GENES, HOMEOBOX; HEART BLOCK; HEART DEFECTS, CONGENITAL; HOMEODOMAIN PROTEINS; HUMANS; MUTATION; TRANSCRIPTION FACTORS;

EID: 4444277258     PISSN: 00086363     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.cardiores.2004.08.001     Document Type: Editorial

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