A novel homozygous mutation in recombination activating gene 2 in 2 relatives with different clinical phenotypes: Omenn syndrome and hyper-IgM syndrome
published in: The Journal of Allergy and Clinical Immunology
date of publication: 2012-07-25
language: English
main subject: Omenn syndrome, homozygosity
Cites articles 9
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Article - wd:Q36438034