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(2010)
Common Variants at 10 Genomic Loci Influence Hemoglobin A(1C) Levels via Glycemic and Nonglycemic Pathways.
DIABETES, 59 (12).
3229 - 3239 (11).
ISSN 0012-1797
https://doi.org/10.2337/db10-0502
SGUL Authors: Strachan, David Peter
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Item Type: |
Article
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Additional Information: |
PubMed ID: 20858683 |
Keywords: |
Adult, Blood Glucose, Body Mass Index, Chromosome Mapping, Cohort Studies, European Continental Ancestry Group, Female, Genetic Variation, Genome-Wide Association Study, Hemoglobin A, Glycosylated, Humans, Male, Meta-Analysis as Topic, Middle Aged, Polymorphism, Single Nucleotide, Science & Technology, Life Sciences & Biomedicine, Endocrinology & Metabolism, NONSPHEROCYTIC HEMOLYTIC-ANEMIA, FASTING GLUCOSE-LEVELS, TYPE-2 DIABETES RISK, GENETIC HEMOCHROMATOSIS, BLOOD-CELLS, ASSOCIATION, MTNR1B, RECLASSIFICATION, POLYMORPHISM, PREVALENCE |
SGUL Research Institute / Research Centre: |
Academic Structure > Population Health Research Institute (INPH) |
Journal or Publication Title: |
DIABETES |
ISSN: |
0012-1797 |
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Dates: |
Date | Event |
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1 December 2010 | Published |
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Web of Science ID: |
WOS:000285988200032 |
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URI: |
https://openaccess.sgul.ac.uk/id/eprint/390 |
Publisher's version: |
https://doi.org/10.2337/db10-0502 |
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