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Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
IntroductionX-linked agammaglobulinemia (XLA) is a humoral immunodeficiency disorder characterized by recurrent infections, severe hypogammaglobulinemia, and a deficiency of circulating B cells. While the hallmark clinical manifestations of XLA typic
Externí odkaz:
https://doaj.org/article/921bd6b34d014954a31c56bc7efc8913