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Article

A New IL-2RG Gene Mutation in an X-linked SCID Identified through TREC/KREC Screening: a Case Report.

Iranian journal of allergy, asthma, and immunology - 1 Aug 2015

Nourizadeh Maryam, Borte Stephan, Fazlollahi Mohammad Reza, Hammarström Lennart, Pourpak Zahra

Abstract excerpt

Severe combined immunodeficiency (SCID) represents a rare group of primary immunodeficiency disorders (PIDs), with known or unknown genetic alterations. Here, we report a new interleukin 2 receptor, gamma chain (IL-2RG) mutation in an Iranian SCID newborn. The patient was a 6-day old boy with a family history of PID. The child was screened using a molecular-based analysis for the assessment of T cell receptor...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 26547715

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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