EIF2AK3 mutations in South Indian children with permanent neonatal diabetes mellitus associated with Wolcott-Rallison syndrome-Reference-Cited by-同舟云学术

EIF2AK3 mutations in South Indian children with permanent neonatal diabetes mellitus associated with Wolcott-Rallison syndrome

Published:2013-10-30 Issue:4 Volume:15 Page:313-318
ISSN:1399-543X
Container-title:Pediatric Diabetes
language:en
Short-container-title:Pediatr Diabetes

Author:

Jahnavi Suresh¹,Poovazhagi Varadarajan²,Kanthimathi Sekar¹,Gayathri Vijay¹,Mohan Viswanathan¹³,Radha Venkatesan¹

Affiliation:

1. Department of Molecular Genetics; Madras Diabetes Research Foundation, ICMR Advanced Centre for Genomics of Type 2 Diabetes and Dr. Mohan's Diabetes Specialities Centre, WHO Collaborating Centre for Non Communicable Diseases Prevention and Control, IDF Centre of Education; Chennai Tamil Nadu India

2. Department of Pediatrics; Institute of Child Health and Hospital for Children; Chennai Tamil Nadu India

3. Department of Diabetology; Dr. Mohan's Diabetes Specialities Centre; Chennai Tamil Nadu India

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology and Child Health,Internal Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/pedi.12089/fullpdf

Reference18 articles.

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2. Infancy-onset diabetes mellitus and multiple epiphyseal dysplasia;Wolcott;J Pediatr,1972

3. Wolcott-Rallison syndrome. Clinical, radiological and histological finding in a Saudi child;Bin-Abbas;Ann Saudi Med,2001

4. Wolcott-Rallison syndrome is the most common genetic cause of permanent neonatal diabetes in consanguineous families;Rubio-Cabezas;J Clin Endocrinol Metab,2009 Nov

5. Loss of kinase activity in a patient with Wolcott-Rallison syndrome caused by a novel mutation in the EIF2AK3 gene;Biason-Lauber;Diabetes,2002 Jul

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