Case Report

Wolcott-Rallison Syndrome Due to a Novel Mutation (R491X) in EIF2AK3 Gene
  • Ercan Mıhçı
  • Doğa Tu¨rkkahraman
  • Sian Ellard
  • Sema Akçurin
  • İffet Bircan
J Clin Res Pediatr Endocrinol 2012; 4: 101-103 DOI: 10.4274/Jcrpe.619 PMID:22672868

Letter to the Editor

Wolcott-Rallison Syndrome with Novel EIF2AK3 Gene Mutation
  • Fatih Gürbüz
  • Bilgin Yüksel
  • Ali Kemal Topaloğlu
J Clin Res Pediatr Endocrinol 2016; 8: 496-497 DOI: 10.4274/jcrpe.3065

Other

Wolcott-Rallison Syndrome
  • Fatih Gürbüz
  • Bilgin Yüksel
  • Ali Kemal Topaloğlu
J Clin Res Pediatr Endocrinol 2015; 7: 84-84

About Journal

Forms

Useful Links

Applications