The val606met mutation in the cardiac beta-myosin heavy chain gene in patients with familial hypertrophic cardiomyopathy is associated with a high risk of sudden death at young age

American Journal of Cardiology

Volumn 87, Issue 11, 2001, Pages 1315-1317

  Havndrup, Ole ^a   Bundgaard, Henning ^a   Andersen, Paal S ^b   Larsen, Lars A ^b   Vuust, Jens ^b   Kjeldsen, Keld ^a   Christiansen, Michael ^b  

^a UNIVERSITY OF COPENHAGEN   (Denmark)

^b STATENS SERUM INSTITUT   (Denmark)

Author keywords

[No Author keywords available]

Indexed keywords

METHIONINE; MYOSIN HEAVY CHAIN; VALINE; DNA GLYCOSYLASE MUTY; DNA GLYCOSYLTRANSFERASE; GLYCOSIDASE; MYOSIN IIB; NONMUSCLE MYOSIN TYPE IIB HEAVY CHAIN;

AGE; ARTICLE; CONTROLLED STUDY; FAMILIAL DISEASE; GENE; GENE MUTATION; HIGH RISK POPULATION; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; INCIDENCE; MAJOR CLINICAL STUDY; MORTALITY; PHENOTYPE; PRIORITY JOURNAL; PROGNOSIS; SUDDEN DEATH; ADOLESCENT; ADULT; CHILD; COHORT ANALYSIS; FEMALE; GENETIC PREDISPOSITION; GENETICS; MALE; METABOLISM; NUCLEOTIDE SEQUENCE; PEDIGREE; RISK; SURVIVAL;

ADOLESCENT; ADULT; AGE FACTORS; CARDIOMYOPATHY, HYPERTROPHIC; CHILD; COHORT STUDIES; DEATH, SUDDEN, CARDIAC; DNA GLYCOSYLASES; DNA MUTATIONAL ANALYSIS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; METHIONINE; MYOSIN HEAVY CHAINS; N-GLYCOSYL HYDROLASES; NONMUSCLE MYOSIN TYPE IIB; PEDIGREE; RISK; SURVIVAL ANALYSIS; VALINE;

EID: 0035354329     PISSN: 00029149     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0002-9149(01)01532-6     Document Type: Article

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