Haplotype-based association study of TCF7L2 gene variants with the development of diabetic retinopathy in an Iranian population-Reference-Cited by-同舟云学术

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Haplotype-based association study of TCF7L2 gene variants with the development of diabetic retinopathy in an Iranian population

Published:2024-03-21 Issue:3 Volume:45 Page:226-232
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Alidoust Leila¹,Sharafshah Alireza²³,Keshavarz Parvaneh²

Affiliation:

1. Department of Medical Genetics, Faculty of Medicine, Guilan University of Medical Sciences, Rasht, Iran

2. Cellular and Molecular Research Center, School of Medicine, Guilan University of Medical Sciences, Rasht, Iran

3. Division of Genetics, Department of Cell and Molecular Biology and Microbiology, Faculty of Science and Biotechnology, University of Isfahan, Isfahan, Iran

Funder

funding associated

Publisher

Informa UK Limited

Link

https://www.tandfonline.com/doi/pdf/10.1080/13816810.2024.2318611

Reference39 articles.

1. The relative contributions of insulin resistance and beta-cell dysfunction to the pathophysiology of Type 2 diabetes

2. The accelerator hypothesis: a review of the evidence for insulin resistance as the basis for type I as well as type II diabetes

3. The worldwide epidemiology of type 2 diabetes mellitus—present and future perspectives

4. Diagnosis and Classification of Diabetes Mellitus

5. Microvascular and Macrovascular Complications of Diabetes

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