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Atypical Omenn Syndrome Due to RAG2 Gene Mutation, a Case Report

Ali Pourvali; Saba Arshi; Mohammad Nabavi; Mohammad Hasan Bemanian; Sima Shokri; Mohammad Shahrooei; Nima Rezaei; Morteza Fallahpour

Volume 16, Issue 4 , December 2019, , Pages 334-338

https://doi.org/10.22034/iji.2019.80285

Abstract
  Severe Combined Immunodeficiency (SCID), characterized by a profound decrease in both the number and function of T cells, is related to more than 20 different mutations. Recombination-activating gene (RAG) 1 and 2 seem to be two of the most common forms presenting with various manifestations, ...  Read More