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Volumn 39, Issue 11, 2016, Pages 1889-1895

Toward precision medicine: TBC1D4 disruption is common among the inuit and leads to underdiagnosis of type 2 diabetes

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CONTROLLED STUDY; FEMALE; GENE; GENE DISRUPTION; GENE FREQUENCY; GENE FUNCTION; GENETIC ASSOCIATION; GENETIC VARIABILITY; GEOGRAPHIC DISTRIBUTION; GLUCOSE BLOOD LEVEL; GLUCOSE METABOLISM; HETEROZYGOTE DETECTION; HUMAN; IMPAIRED GLUCOSE TOLERANCE; INSULIN BLOOD LEVEL; INUIT; LONGITUDINAL STUDY; MAJOR CLINICAL STUDY; MALE; NON INSULIN DEPENDENT DIABETES MELLITUS; NONSENSE MUTATION; PERSONALIZED MEDICINE; POPULATION GENETICS; PREVALENCE; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM; TBC1D4 GENE; ALASKA; CANADA; DIABETES MELLITUS, TYPE 2; DNA SEQUENCE; GENETICS; GLUCOSE TOLERANCE TEST; GREENLAND; HYPERGLYCEMIA; METABOLISM; MIDDLE AGED; POSTPRANDIAL STATE; PREDIABETIC STATE; STOP CODON;

EID: 84994381404     PISSN: 01495992     EISSN: 19355548     Source Type: Journal    
DOI: 10.2337/dc16-0769     Document Type: Article
Times cited : (32)

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