IL2RG hypomorphic mutation: identification of a novel pathogenic mutation in exon 8 and a review of the literature
Abstract Background Atypical X-linked severe combined immunodeficiency (X-SCID) is a variant of cellular immunodeficiency due to hypomorphic mutations in the interleukin 2 receptor gamma (IL2RG) gene. Due to a leaky clinical phenotype, diagnosis and appropriate treatment are challenging in these pat...
Main Authors: | , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2019-01-01
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Series: | Allergy, Asthma & Clinical Immunology |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s13223-018-0317-y |