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

Jahnavi, S and Poovazhagi, V and Kanthimathi, S and Gayathri, V and Mohan, V and Radha, V (2014) EIF2AK3 mutations in South Indian children with permanent neonatal diabetes mellitus associated with Wolcott-Rallison syndrome. Pediatric diabetes, 15 (4). pp. 313-8. ISSN 1399-5448

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Abstract

This study describes the clinical and genetic evaluation of permanent neonatal diabetes due to Wolcott-Rallison syndrome (WRS) in south Indian consanguineous families. We aimed to evaluate the genetic basis of the disease in eight children with WRS from five South Indian families.

Item Type:Article
Official URL/DOI:http://onlinelibrary.wiley.com/doi/10.1111/pedi.12...
Uncontrolled Keywords:EIF2AK3; PERK; PNDM; WRS; neonatal diabetes
Subjects:Diabetes > Diabetes Risk Factors
Genetics and Diabetes
Divisions:Neonatal Diabetes
Department of Advanced Research Biochemistry
ID Code:859
Deposited By:surendar radha
Deposited On:06 Nov 2014 10:40
Last Modified:06 Nov 2014 10:40

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