Association between FTO, MC4R, SLC30A8, and KCNQ1 gene variants and type 2 diabetes in Saudi population

Genetics and Molecular Research

Volumn 13, Issue 4, 2014, Pages 10194-10203

  Bazzi, M D ^a   Nasr, F A ^a   Alanazi, M S ^a   Alamri, A ^a   Turjoman, A A ^b   Moustafa, A S ^b   Alfadda, A A ^b   Pathan, A A K ^a   Parine, N R ^a  

^a KING SAUD UNIVERSITY   (Saudi Arabia)

^b KING SAUD UNIVERSITY   (Saudi Arabia)

Author keywords

Ethnicity; Fat mass and obesity associated; Polymorphisms; Solute carrier family 30 member 8; Type 2 diabetes mellitus

Indexed keywords

MELANOCORTIN 4 RECEPTOR; CATION TRANSPORT PROTEIN; FTO PROTEIN, HUMAN; KCNQ1 PROTEIN, HUMAN; MC4R PROTEIN, HUMAN; POTASSIUM CHANNEL KCNQ1; PROTEIN; SLC30A8 PROTEIN, HUMAN;

ADULT; ARTICLE; CONTROLLED STUDY; ETHNICITY; FEMALE; FTO GENE; GENE; GENE FREQUENCY; GENE LOCUS; GENETIC ASSOCIATION; GENETIC VARIABILITY; HUMAN; KCNQ1 GENE; MAJOR CLINICAL STUDY; MALE; MC4R GENE; NON INSULIN DEPENDENT DIABETES MELLITUS; PHYSICAL EXAMINATION; PLESIOMORPHY; SAUDI; SAUDI ARABIA; SINGLE NUCLEOTIDE POLYMORPHISM; SLC30A8 GENE; CASE CONTROL STUDY; GENETIC PREDISPOSITION; GENETICS; GENOTYPE; MIDDLE AGED;

ADULT; CASE-CONTROL STUDIES; CATION TRANSPORT PROTEINS; DIABETES MELLITUS, TYPE 2; FEMALE; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HUMANS; KCNQ1 POTASSIUM CHANNEL; MALE; MIDDLE AGED; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEINS; RECEPTOR, MELANOCORTIN, TYPE 4; SAUDI ARABIA;

EID: 84919360738     PISSN: None     EISSN: 16765680     Source Type: Journal    
DOI: 10.4238/2014.December.4.14     Document Type: Article

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