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5. Wolcott-Rallison Syndrome with Novel EIF2AK3 Gene Mutation. Gürbüz F; Yüksel B; Topaloğlu AK J Clin Res Pediatr Endocrinol; 2016 Dec; 8(4):496-497. PubMed ID: 27145240 [No Abstract] [Full Text] [Related]
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11. Wolcott Rallison syndrome: a rare inherited diabetes mellitus. Khare S; Goroshi MR; Budyal S; Bandgar T; Lila A; Shah N Indian J Pediatr; 2014 Nov; 81(11):1225-7. PubMed ID: 24710710 [TBL] [Abstract][Full Text] [Related]
12. A Genotype-First Approach for Clinical and Genetic Evaluation of Wolcott-Rallison Syndrome in a Large Cohort of Iranian Children With Neonatal Diabetes. Abbasi F; Habibi M; Enayati S; Bitarafan F; Razzaghy-Azar M; Sotodeh A; Omran SP; Maroofian R; Amoli MM Can J Diabetes; 2018 Jun; 42(3):272-275. PubMed ID: 28843469 [TBL] [Abstract][Full Text] [Related]
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14. A novel EIF2AK3 mutation leading to Wolcott-Rallison syndrome in a Chinese child. Sang Y; Liu M; Yang W; Yan J; Chengzhu ; Ni G J Pediatr Endocrinol Metab; 2011; 24(3-4):181-4. PubMed ID: 21648287 [TBL] [Abstract][Full Text] [Related]
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