Common variation in the LMNA gene (encoding lamin A/C) and type 2 diabetes: Association analyses in 9,518 subjects

Diabetes

Volumn 56, Issue 3, 2007, Pages 879-883

  Owen, Katharine R ^a   Groves, Christopher J ^a   Hanson, Robert L ^b   Knowler, William C ^b   Shuldiner, Alan R ^c   Elbein, Steven C ^d,e   Mitchell, Braxton D ^c   Froguel, Philippe ^f,g   Ng, Maggie C Y ^h,i   Chan, Juliana C ⁱ   Jia, Weiping ^j   Deloukas, Panos ^k   Hitman, Graham A ^l   Walker, Mark ^m   Frayling, Timothy M ⁿ   Hattersley, Andrew T ⁿ   Zeggini, Eleftheria ^a,o   McCarthy, Mark I ^a,o  

^a UNIVERSITY OF OXFORD   (United Kingdom)

^b NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES   (United States)

^c UNIVERSITY OF MARYLAND SCHOOL OF MEDICINE   (United States)

^d CENTRAL ARKANSAS VETERANS HEALTHCARE SYSTEM   (United States)

^e UNIVERSITY OF ARKANSAS FOR MEDICAL SCIENCES   (United States)

^f INSTITUT DE BIOLOGIE DE LILLE   (France)

^g IMPERIAL COLLEGE LONDON   (United Kingdom)

^h UNIVERSITY OF CHICAGO   (United States)

ⁱ CHINESE UNIVERSITY OF HONG KONG   (Hong Kong)

^j SHANGHAI JIAO TONG UNIVERSITY AFFILIATED SIXTH PEOPLE S HOSPITAL   (China)

^k WELLCOME TRUST SANGER INSTITUTE   (United Kingdom)

^l QUEEN MARY UNIVERSITY OF LONDON   (United Kingdom)

^m NEWCASTLE UNIVERSITY   (United Kingdom)

ⁿ PENINSULA MEDICAL SCHOOL   (United Kingdom)

^o UNIVERSITY OF OXFORD   (United Kingdom)

more..

Author keywords

[No Author keywords available]

Indexed keywords

INSULIN; LAMIN A; LAMIN C; ORAL ANTIDIABETIC AGENT;

ADULT; ARTICLE; CHROMOSOME 1Q; CONTROLLED STUDY; DISEASE PREDISPOSITION; FEMALE; GENE FREQUENCY; GENE MAPPING; GENE MUTATION; GENETIC LINKAGE; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HUMAN; INSULIN RESISTANCE; LIPODYSTROPHY; MAJOR CLINICAL STUDY; MALE; METABOLIC SYNDROME X; NON INSULIN DEPENDENT DIABETES MELLITUS; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

ADULT; AGED; CASE-CONTROL STUDIES; DIABETES MELLITUS, TYPE 2; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HUMANS; LAMIN TYPE A; MALE; MIDDLE AGED; MUTATION; ODDS RATIO; POLYMORPHISM, SINGLE NUCLEOTIDE; VARIATION (GENETICS);

EID: 33847357832     PISSN: 00121797     EISSN: 00121797     Source Type: Journal    
DOI: 10.2337/db06-0930     Document Type: Article

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