A Genotype-First Approach for Clinical and Genetic Evaluation of Wolcott-Rallison Syndrome in a Large Cohort of Iranian Children With Neonatal Diabetes-Reference-Cited by-同舟云学术

A Genotype-First Approach for Clinical and Genetic Evaluation of Wolcott-Rallison Syndrome in a Large Cohort of Iranian Children With Neonatal Diabetes

Published:2018-06 Issue:3 Volume:42 Page:272-275
ISSN:1499-2671
Container-title:Canadian Journal of Diabetes
language:en
Short-container-title:Canadian Journal of Diabetes

Author:

Abbasi Farzaneh,Habibi Maryam,Enayati Samaneh,Bitarafan Fatemeh,Razzaghy-Azar Maryam,Sotodeh Aria,Omran Sima Parvizi,Maroofian Reza,Amoli Mahsa M.

Publisher

Elsevier BV

Subject

Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism,Internal Medicine

Reference18 articles.

1. A novel EIF2AK3 mutation leading to Wolcott-Rallison syndrome in a Chinese child;Sang;J Pediatr Endocrinol Metab,2011

2. Novel mutation in Wolcott-Rallison syndrome with variable expression in two Omani siblings;Al-Sinani;Oman Med J,2015

3. Wolcott-Rallison syndrome;Julier;Orphanet J Rare Dis,2010

4. Early-onset diabetes mellitus and neurodevelopmental retardation: The first Greek case of Wolcott-Rallison syndrome;Triantafyllou;J Pediatr Endocrinol Metab,2014

5. Variable phenotype in five patients with Wolcott-Rallison syndrome due to the same EIF2AK3 (c.1259delA) mutation;Al-Shawi;J Pediatr Endocrinol Metab,2013

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