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Volumn 101, Issue 4, 2015, Pages 294-301

Novel genotype-phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathy

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGE DISTRIBUTION; AGED; ANK2 GENE; ARTICLE; CARDIOVASCULAR MORTALITY; CHILD; CLINICAL EXAMINATION; CONTROLLED STUDY; FAMILY HISTORY; FEMALE; GENE; GENE MUTATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPE PHENOTYPE CORRELATION; HEART VENTRICLE HYPERTROPHY; HIGH THROUGHPUT SEQUENCING; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; INCIDENCE; MAJOR CLINICAL STUDY; MALE; OVERALL SURVIVAL; PRESCHOOL CHILD; PREVALENCE; PROSPECTIVE STUDY; SCHOOL CHILD; SEX DIFFERENCE; SP GENE; SUDDEN CARDIAC DEATH; VERY ELDERLY; AGE; CARDIOMYOPATHY, HYPERTROPHIC, FAMILIAL; DEATH, SUDDEN, CARDIAC; DNA MUTATIONAL ANALYSIS; ENGLAND; GENETIC ASSOCIATION STUDY; GENETIC PREDISPOSITION; GENETICS; KAPLAN MEIER METHOD; MIDDLE AGED; MORTALITY; MUTATION; PEDIGREE; PHENOTYPE; PREDICTIVE VALUE; PROCEDURES; RETROSPECTIVE STUDY; RISK FACTOR; YOUNG ADULT;

EID: 84921912496     PISSN: 13556037     EISSN: 1468201X     Source Type: Journal    
DOI: 10.1136/heartjnl-2014-306387     Document Type: Article
Times cited : (123)

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