the common c49620t polymorphism in the sulfonylurea receptor gene sur1 (abcc8) in patients with gestational diabetes and subsequent glucose metabolism abnormalities共同c49620t磺酰脲类受体基因的多态性sur1(abcc8)妊娠期糖尿病患者和随后的葡萄糖代谢异常.pdfVIP

Hindawi Publishing Corporation Experimental Diabetes Research Volume 2012, Article ID 712617, 7 pages doi:10.1155/2012/712617 Clinical Study The Common C49620T Polymorphism in the Sulfonylurea Receptor Gene SUR1 (ABCC8) in Patients with Gestational Diabetes and Subsequent Glucose Metabolism Abnormalities 1 ´ 2 1 Piotr Mole¸da, Agnieszka Binczak-Kuleta, Katarzyna Homa, 3 4 5 ´ 1 Krzysztof Safranow, Zbigniew Celewicz, Anhelli Syrenicz, Adam Stefanski, Aneta Fronczyk,1 and Lilianna Majkowska1 1 Department of Diabetology and Internal Diseases, Pomeranian Medical University, Szczecin, Poland 2 Chair of Clinical Biochemistry and Laboratory Diagnostics, Pomeranian Medical University, Szczecin, Poland 3 Chair of Biochemistry and Medical Chemistry, Pomeranian Medical University, Szczecin, Poland 4 Department of Maternal-Fetal Medicine and Gynecology, Pomeranian Medical University, Szczecin, Poland 5 Department of Endocrinology, Metabolic and Internal Diseases, Pomeranian Medical University, Szczecin, Poland Correspondence should be addressed to Piotr Mole¸da, pmoleda@wp.pl Received 5 February 2012; Accepted 9 July 2012 Academic Editor: Asli F. Ceylan-Isik Copyright © 2012 Piotr Mole¸da et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Aim . The aim of this study is to investigate the relationship between the common C49620T polymorphism in the sulfonylurea r