QT dispersion in α-myosin heavy-chain familial hypertrophic cardiomyopathy mice

Pediatric Research

Volumn 45, Issue 5, 1999, Pages 643-647

  Bevilacqua, Laura M ^a,c   Maguire, Colin T ^a,c   Seidman, Jonathan G ^b,c   Seidman, Christine E ^b,c   Berul, Charles I ^a,c  

^a BOSTON CHILDREN S HOSPITAL   (United States)

^b Howard Hughes Medical Center   (United States)

^c HARVARD MEDICAL SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARRHYTHMOGENESIS; ARTICLE; CONTROLLED STUDY; FAMILIAL DISEASE; FEMALE; GENDER; HEART VENTRICLE ARRHYTHMIA; HYPERTROPHIC CARDIOMYOPATHY; MALE; MOUSE; NONHUMAN; PRIORITY JOURNAL; QT INTERVAL; RISK ASSESSMENT; RISK FACTOR;

AMINO ACID SUBSTITUTION; ANIMALS; BODY SURFACE POTENTIAL MAPPING; CARDIOMYOPATHY, HYPERTROPHIC; FEMALE; HEART; HEART RATE; LONG QT SYNDROME; MALE; MICE; MICE, MUTANT STRAINS; MYOSIN HEAVY CHAINS; PHENOTYPE; REFERENCE VALUES; RISK FACTORS; SEX CHARACTERISTICS; TACHYCARDIA, VENTRICULAR;

EID: 0032907451     PISSN: 00313998     EISSN: 15300447     Source Type: Journal    
DOI: 10.1203/00006450-199905010-00005     Document Type: Article

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