Genetics of atrioventricular conduction disease in humans

Anatomical Record - Part A Discoveries in Molecular, Cellular, and Evolutionary Biology

Volumn 280, Issue 2, 2004, Pages 934-939

  Benson, D Woodrow ^a  

^a CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER   (United States)

Author keywords

Congenital heart disease; Gene mutation; Heart block; Human genetics; Ion channels; Pediatrics; Transcription factors

Indexed keywords

HYDROXYMETHYLGLUTARYL COENZYME A REDUCTASE KINASE; ION CHANNEL;

ATRIOVENTRICULAR BLOCK; ATRIOVENTRICULAR CONDUCTION; AUTOSOMAL DOMINANT INHERITANCE; CARDIOVASCULAR RISK; CONFERENCE PAPER; CONGENITAL HEART MALFORMATION; DISEASE ASSOCIATION; ENZYME SUBUNIT; GENE EXPRESSION; GENE MUTATION; GENETIC HETEROGENEITY; GENETIC MODEL; HEART MUSCLE CELL; HEART VENTRICLE HYPERTROPHY; HUMAN; IDIOPATHIC DISEASE; NEUROMUSCULAR DISEASE; OPEN HEART SURGERY; PENETRANCE; PRIORITY JOURNAL; WOLFF PARKINSON WHITE SYNDROME;

ANIMALS; ATRIOVENTRICULAR NODE; HEART BLOCK; HEART CONDUCTION SYSTEM; HEART DEFECTS, CONGENITAL; HOMEODOMAIN PROTEINS; HUMANS; NEUROMUSCULAR DISEASES; SODIUM CHANNELS;

EID: 4844228952     PISSN: 0003276X     EISSN: None     Source Type: Journal    
DOI: 10.1002/ar.a.20099     Document Type: Conference Paper

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