Genetic research in Immunogenetics Group of Endocrinology and Metabolism Research Institute
Author:
Funder
Endocrinology and Metabolism Research Center, Tehran University of Medical Sciences
Publisher
Springer Science and Business Media LLC
Subject
Endocrinology, Diabetes and Metabolism,Internal Medicine
Link
http://link.springer.com/content/pdf/10.1007/s40200-021-00753-y.pdf
Reference57 articles.
1. Abbasi F, Saba S, Ebrahim-Habibi A, Sayahpour FA, Amiri P, Larijani B, et al. Detection of KCNJ11 gene mutations in a family with neonatal diabetes mellitus. Mol Diagn Ther. 2012;16(2):109–14.
2. Alimadadi A, Ebrahim-Habibi A, Abbasi F, Amoli M, Sayahpour FA, Larijani B. Novel mutations of wolframin: a report with a look at the protein structure. Clin Genet. 2011;79(1):96–9.
3. Abbasi R, Bitarafan F, Khodaeian M, Ebrahim-Habibi A, Abbasi F, Amoli MM. Molecular investigation of WFS1 gene exon 8 in Iranian patients with Wolfram syndrome. Int J Diabetes Dev Ctries. 2016;36(1):75–80.
4. Sahebi L, Niknafs N, Dalili H, Amini E, Esmaeilnia T, Amoli M, et al. Iranian neonatal diabetes mellitus due to mutation in PDX1 gene: a case report. J Med Case Rep. 2019;13(1):258.
5. Ranjbar SH, Amiri P, Amoli MM, Soltani A. A new mitochondrial mutation in a patient with diabetes mellitus, deafness, hydronephrosis and joint contractures. J Pediatr Endocrinol Metab. 2008;21(12):1185–90.
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