Association of a polymorphic variant of the Werner helicase gene with myocardial infarction in a Japanese population

American Journal of Medical Genetics

Volumn 68, Issue 4, 1997, Pages 494-498

  Ye, L ^a   Miki, T ^a   Nakura, J ^a   Oshima, J ^a   Kamino, K ^a   Rakugi, H ^a   Ikegami, H ^a   Higaki, J ^a   Edland, S D ^a   Martin, G M ^a   Ogihara, T ^a  

^a OSAKA UNIVERSITY MEDICAL SCHOOL   (Japan)

Author keywords

diabetes mellitus; myocardial infarction; Werner syndrome

Indexed keywords

HELICASE;

ADULT; ARTICLE; CONTROLLED STUDY; FEMALE; GENOTYPE; HEART INFARCTION; HOMOZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; MALE; NON INSULIN DEPENDENT DIABETES MELLITUS; PRIORITY JOURNAL; WERNER SYNDROME;

ADULT; AGE OF ONSET; AGED; ARGININE; CASE-CONTROL STUDIES; CYSTEINE; DIABETES MELLITUS, TYPE 2; FEMALE; HOMOZYGOTE; HUMANS; JAPAN; MALE; MIDDLE AGED; MUTATION; MYOCARDIAL INFARCTION; POLYMORPHISM, GENETIC; VARIATION (GENETICS); WERNER SYNDROME;

EID: 17344379792     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19970211)68:4<494::AID-AJMG30>3.0.CO;2-L     Document Type: Article

References (27)