Strong parent-of-Origin effects in the association of kcnq1 variants with type 2 diabetes in american indians

Diabetes

Volumn 62, Issue 8, 2013, Pages 2984-2991

  Hanson, Robert L ^a   Guo, Tingwei ^a   Muller, Yunhua L ^a   Fleming, Jamie ^a   Knowler, William C ^a   Kobes, Sayuko ^a   Bogardus, Clifton ^a   Baier, Leslie J ^a  

^a Digestive and Kidney Diseases   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GLUCOSE; POTASSIUM CHANNEL KCNQ1; HCCA2 PROTEIN, HUMAN; INSULIN; KCNQ1 PROTEIN, HUMAN; KLF14 PROTEIN, HUMAN; NERVE PROTEIN; TRANSCRIPTION FACTOR SP;

ADULT; ALLELE; AMERICAN INDIAN; ARTICLE; CONTROLLED STUDY; FEMALE; GENETIC ASSOCIATION; GENETIC TRAIT; GENETIC VARIABILITY; GLUCOSE BLOOD LEVEL; HAPLOTYPE; HUMAN; INSULIN RELEASE; INTRAVENOUS GLUCOSE TOLERANCE TEST; MAJOR CLINICAL STUDY; MALE; METABOLISM; NON INSULIN DEPENDENT DIABETES MELLITUS; NUCLEAR FAMILY; PARENT; PARENT OF ORIGIN EFFECT; PARENTAGE ANALYSIS; PRIORITY JOURNAL; GENETIC PREDISPOSITION; GENETICS; GENOTYPE; GLUCOSE TOLERANCE TEST; LONGITUDINAL STUDY; SECRETION (PROCESS); SINGLE NUCLEOTIDE POLYMORPHISM;

ADULT; ALLELES; DIABETES MELLITUS, TYPE 2; FEMALE; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; GLUCOSE TOLERANCE TEST; HAPLOTYPES; HUMANS; INDIANS, NORTH AMERICAN; INSULIN; KCNQ1 POTASSIUM CHANNEL; LONGITUDINAL STUDIES; MALE; NERVE TISSUE PROTEINS; PARENTS; POLYMORPHISM, SINGLE NUCLEOTIDE; SP TRANSCRIPTION FACTORS;

EID: 84891676958     PISSN: 00121797     EISSN: 1939327X     Source Type: Journal    
DOI: 10.2337/db12-1767     Document Type: Article

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