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Article

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

Pediatric diabetes - 1 Jun 2014

Jahnavi Suresh, Poovazhagi Varadarajan, Kanthimathi Sekar, Gayathri Vijay, Mohan Viswanathan, Radha Venkatesan

Abstract excerpt

OBJECTIVE: 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. PATIENTS AND METHODS: We studied eight children who presented with permanent neonatal diabetes from five South Indian...

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Source

Identifiers

PMID: 24168455
DOI: 10.1111/pedi.12089

Genes

ABCC8
GCK
INS
KCNJ11

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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