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Elsevier, Journal of Allergy and Clinical Immunology, 6(130), p. 1414-1416, 2012

DOI: 10.1016/j.jaci.2012.06.012

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A novel homozygous mutation in recombination activating gene 2 in 2 relatives with different clinical phenotypes: Omenn syndrome and hyper-IgM syndrome

This paper is available in a repository.
This paper is available in a repository.

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