Association between genetic variants and characteristic symptoms of type 2 diabetes: A matched case-control study

Association between genetic variants and characteristic symptoms of type 2 diabetes: A matched... Chin J Integr Med 2017 Jun;23(6):415-424 • • Available online at link.springer.com/journal/11655 hinese Journal of Integrative Medicine Journal homepage: www.cjim.cn/zxyjhen/zxyjhen/ch/index.aspx E-mail: cjim_en@cjim.cn Original Article Association between Genetic Variants and Characteristic Symptoms of Type 2 Diabetes: A Matched Case-Control Study 1 1 1 2 2 DOU Hao-ying , WANG Yuan-yuan , YANG Nan , HENG Ming-li , ZHOU Xuan , 2 2 2 3 2 BU Huai-en , XU Fang , ZHAO Tie-niu , HUANG He , and WANG Hong-wu A ABSTRACT BSTRACT Objective Objective:: To examine the association of genetic variants with characteristic symptoms of type 2 To examine the association of genetic variants with characteristic symptoms of type 2 M Methods ethods d diabetes mellitus (T2DM). iabetes mellitus (T2DM). :: A matched case-control study was performed to investigate the association A matched case-control study was performed to investigate the association b between common variants in four genes (CDKAL1, GLIS3, GRK5, and TCF7L2) and symptoms of T2DM. etween common variants in four genes (CDKAL1, GLIS3, GRK5, and TCF7L2) and symptoms of T2DM. S Symptoms were examined with questionnaire for 710 subjects. Genomic DNA was extracted from peripheral blood ymptoms were examined with questionnaire for 710 subjects. Genomic DNA was http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Chinese Journal of Integrative Medicine Springer Journals

Association between genetic variants and characteristic symptoms of type 2 diabetes: A matched case-control study

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Publisher
Springer Berlin Heidelberg
Copyright
Copyright © 2015 by Chinese Association of the Integration of Traditional and Western Medicine and Springer-Verlag Berlin Heidelberg
Subject
Medicine & Public Health; Medicine/Public Health, general
ISSN
1672-0415
eISSN
1993-0402
D.O.I.
10.1007/s11655-015-2290-3
Publisher site
See Article on Publisher Site

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