Myosin light chain mutation causes autosomal recessive cardiomyopathy with mid-cavitary hypertrophy and restrictive physiology

Circulation

Volumn 105, Issue 20, 2002, Pages 2337-2340

  Olson, Timothy M ^a   Karst, Margaret L ^a   Whitby, Frank G ^b   Driscoll, David J ^a  

^a MAYO CLINIC   (United States)

^b UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

Author keywords

Cardiomyopathy; Genetics; Myosin

Indexed keywords

DNA; MYOSIN LIGHT CHAIN;

ADOLESCENT; ADULT; AGED; AMINO ACID SUBSTITUTION; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CARDIOMYOPATHY; CASE REPORT; ELECTROCARDIOGRAM; FEMALE; GENETIC COUNSELING; GENOTYPE; HOMOZYGOSITY; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; MALE; MUTATION; PATHOGENESIS; PEDIGREE; PRIORITY JOURNAL; SCHOOL CHILD; SIBLING;

ADOLESCENT; ADULT; AGE OF ONSET; AGED; AGED, 80 AND OVER; ALLELES; AMINO ACID SUBSTITUTION; CARDIOMYOPATHY, HYPERTROPHIC, FAMILIAL; CONSANGUINITY; CONSERVED SEQUENCE; DNA MUTATIONAL ANALYSIS; ECHOCARDIOGRAPHY; ELECTROCARDIOGRAPHY; FEMALE; GENES, RECESSIVE; GENOTYPE; HAPLOTYPES; HETEROZYGOTE DETECTION; HOMOZYGOTE; HUMANS; LINKAGE (GENETICS); MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; MYOSIN LIGHT CHAINS; PEDIGREE; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL;

EID: 0037150221     PISSN: 00097322     EISSN: None     Source Type: Journal    
DOI: 10.1161/01.CIR.0000018444.47798.94     Document Type: Article

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