Cardiac troponin T lysine 210 deletion in a family with dilated cardiomyopathy

Journal of Cardiac Failure

Volumn 8, Issue 1, 2002, Pages 28-32

  Hanson, Emily L ^a   Jakobs, Petra M ^a   Keegan, Hugh ^a   Coates, Kelly ^a   Bousman, Sylvia ^a   Dienel, Nicholas H ^b   Litt, Michael ^a   Hershberger, Ray E ^a  

^a OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

^b Rogue Valley Medical Center   (United States)

Author keywords

Familial dilated cardiomyopathy; Genetics; Heart failure; Sudden cardiac death

Indexed keywords

LYSINE; TROPONIN T;

ADOLESCENT; ADULT; AGED; ARTICLE; ATRIOVENTRICULAR BLOCK; AUTOSOMAL DISORDER; BASE PAIRING; CHILD; DISEASE ASSOCIATION; DISEASE COURSE; DISEASE SEVERITY; EXON; FAMILIAL DISEASE; FEMALE; GENE DELETION; GENE FREQUENCY; GENE MUTATION; HEART ATRIUM FIBRILLATION; HEART DEATH; HEART DILATATION; HEART FAILURE; HEART MUSCLE CONDUCTION SYSTEM; HUMAN; IDIOPATHIC DISEASE; MAJOR CLINICAL STUDY; MALE; ONSET AGE; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; SUDDEN DEATH;

EID: 0036174030     PISSN: 10719164     EISSN: None     Source Type: Journal    
DOI: 10.1054/jcaf.2002.31157     Document Type: Article

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