Associated Papers
HLH and Recurrent EBV Lymphoma as the presenting manifestation of MAGT1 Deficiency: A Systematic Review of the Expanding Disease Spectrum.
Golloshi K et al.
Journal of Clinical Immunology, 2024
Diversity of XMEN Disease: Description of 2 Novel Variants and Analysis of the Lymphocyte Phenotype.
Klinken EM et al.
Journal of Clinical Immunology, 2020
Mutations in MAGT1 lead to a glycosylation disorder with a variable phenotype.
Blommaert E et al.
Proceedings of the National Academy of Sciences of the United States of America, 2019
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