Assigning a causal role to genetic variants in hypertrophic cardiomyopathy

Circulation: Cardiovascular Genetics

Volumn 6, Issue 1, 2013, Pages 2-4

  Watkins, Hugh ^a  

^a UNIVERSITY OF OXFORD   (United Kingdom)

Author keywords

Genetics; Genomics; Hypertrophic cardiomyopathy; Mutation; Polymorphism

Indexed keywords

CONNECTIN; MYOSIN HEAVY CHAIN ALPHA; TROPONIN C;

ACTIN FILAMENT; CONGESTIVE CARDIOMYOPATHY; DNA SEQUENCE; GENE EXPRESSION; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENE MUTATION; GENETIC ASSOCIATION; GENETIC CONSERVATION; GENETIC SCREENING; GENETIC VARIABILITY; HAPLOTYPE; HEART RIGHT VENTRICLE DYSPLASIA; HYPERTROPHIC CARDIOMYOPATHY; LONG QT SYNDROME; MISSENSE MUTATION; MYOFILAMENT; PHENOTYPE; PRIORITY JOURNAL; PROTEIN STRUCTURE; REVIEW; SINGLE NUCLEOTIDE POLYMORPHISM; SPLICING DEFECT;

CARDIOMYOPATHY, HYPERTROPHIC; FEMALE; HUMANS; MALE; MICROFILAMENT PROTEINS; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 84878079227     PISSN: 1942325X     EISSN: 19423268     Source Type: Journal    
DOI: 10.1161/CIRCGENETICS.111.000032     Document Type: Review

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