Molecular investigation of WFS1 gene exon 8 in Iranian patients with Wolfram syndrome-Reference-Cited by-同舟云学术

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Molecular investigation of WFS1 gene exon 8 in Iranian patients with Wolfram syndrome

Published:2015-08-13 Issue:1 Volume:36 Page:75-80
ISSN:0973-3930
Container-title:International Journal of Diabetes in Developing Countries
language:en
Short-container-title:Int J Diabetes Dev Ctries

Author:

Abbasi Roshanak,Bitarafan Fatemeh,Khodaeian Mehrnoosh,Ebrahim-Habibi Azadeh,Abbasi Farzaneh,Amoli Mahsa M.

Publisher

Springer Science and Business Media LLC

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

Link

http://link.springer.com/content/pdf/10.1007/s13410-015-0425-x.pdf

Reference44 articles.

1. Kumar S. Wolfram syndrome: important implications for pediatricians and pediatric endocrinologists. Pediatr Diabetes. 2010;11:28–37.

2. Barrett TG, Bundey SE, Macleod AF. Neurodegeneration and diabetes: UK nationwide study of Wolfram (DIDMOAD) syndrome. Lancet. 1995;346:1458–63.

3. Valsalan R, Gonsalves H, Mailankot M, Mulamani N, Sheshadri S. Wolfram syndrome - clinical and diagnostic details. Indian J Clin Biochem. 2009;24(4):436–8.

4. Kinsley BT, Swift M, Dumont RH, Swift RG. Morbidity and mortality in the Wolfram syndrome. Diabetes Care. 1995;18:1566–70.

5. Simsek E, Simsek T, Tekgul S, Hosal S, Seyrantepe V, Aktan G. Wolfram (DIDMOAD) syndrome: a multidisciplinary clinical study in nine Turkish patients and review of the literature. Acta Paediatr. 2003;92:55–61.

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3. A homozygous missense mutation ofWFS1gene causes Wolfram's syndrome without hearing loss in an Iranian family (a report of clinical heterogeneity);Journal of Clinical Laboratory Analysis;2020-05-17

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