Lack of replication of common EXT2 gene variants with susceptibility to type 2 diabetes in Lebanese Arabs

Diabetes and Metabolism

Volumn 39, Issue 6, 2013, Pages 532-536

  Nemr, R ^a   Al Busaidi, A S ^b   Sater, M S ^b   Echtay, A ^c   Saldanha, F L ^b   Racoubian, E ^d   Keleshian, S H ^e   Almawi, W Y ^b  

^a RIZK HOSPITAL   (Lebanon)

^b ARABIAN GULF UNIVERSITY   (Bahrain)

^c RAFIC HARIRI UNIVERSITY HOSPITAL   (Lebanon)

^d St Marc Medical Center   (Lebanon)

^e HAIGAZIAN UNIVERSITY   (Lebanon)

Author keywords

Diabetes; Exostosin 2; Haplotypes; Replication studies

Indexed keywords

EXOSTOSIN 2; GLYCOSYLTRANSFERASE; UNCLASSIFIED DRUG;

ADULT; AGED; ALLELIC EXCLUSION; ARAB; ARTICLE; BODY MASS; CASE CONTROL STUDY; CONTROLLED STUDY; FEMALE; GENE FREQUENCY; GENE REPLICATION; GENETIC ASSOCIATION; GENETIC MODEL; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HUMAN; LEBANON; MAJOR CLINICAL STUDY; MALE; NON INSULIN DEPENDENT DIABETES MELLITUS; SINGLE NUCLEOTIDE POLYMORPHISM;

DIABETES; DIABÈTE; EXOSTOSIN-2; EXOSTOSINE; HAPLOTYPE; HAPLOTYPES; REPLICATION STUDIES;

ARABS; CASE-CONTROL STUDIES; COMORBIDITY; DIABETES MELLITUS, TYPE 2; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HAPLOTYPES; HUMANS; LEBANON; MALE; MIDDLE AGED; N-ACETYLGLUCOSAMINYLTRANSFERASES; OBESITY; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 84887620510     PISSN: 12623636     EISSN: 18781780     Source Type: Journal    
DOI: 10.1016/j.diabet.2013.05.001     Document Type: Article

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