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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.
The X-linked hyper-IgM syndrome: clinical and immunologic features of 79 patients.
Hyper IgM Syndrome: a Report from the USIDNET Registry.
Models of Human Immunodeficiencies
Hyper IgM Immunodeficiency Syndrome Type 1