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Dergiler / Journal of Clinical Research in Pediatric Endocrinology / 2016 / Cilt: 8 - Sayı: 4

Wolcott-Rallison Syndrome with Novel EIF2AK3 Gene Mutation

FATİH GÜRBÜZ
BİLGİN YÜKSEL
Ali Kemal TOPALOĞLU
Sayfa
496–497
DOI
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GÜRBÜZ, F., YÜKSEL, B., TOPALOĞLU, A. K. (2016). Wolcott-Rallison Syndrome with Novel EIF2AK3 Gene Mutation. Journal of Clinical Research in Pediatric Endocrinology, Cilt: 8 - Sayı: 4, 496–497. https://ajindex.com/articles/216337

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Kaynakça (3)

  1. Wolcott CD, Rallison ML. Infancy-onset diabetes mellitus and multiple epiphyseal dysplasia. J Pediatr 1972;80:292-297.
  2. Mihci E, Turkkahraman D, Ellard S, Akcurin S, Bircan I. Wolcott-Rallison syndrome due to a novel mutation (R491X) in EIF2AK3 gene. J Clin Res Pediatr Endocrinol 2012;4:101-103.
  3. Ozbek MN, Senee V, Aydemir S, Kotan LD, Mungan NO, Yuksel B, Julier C, Topaloglu AK. Wolcott-Rallison syndrome due to the same mutation (W522X) in EIF2AK3 in two unrelated families and review of the literature. Pediatr Diabetes 2010;11:279-285. Epub 2010 Feb 25. Julier C, Nicolino M. Wolcott-Rallison syndrome. Orphanet J Rare Dis 2010;5:29. Juneja A, Sultan A, Bhatnagar S. Wolcott-Rallison syndrome. J Indian Soc Pedod Prev Dent 2012;30:250-253.