Distinct Clinical Features and Novel Mutations in Taiwanese Patients With X-Linked Agammaglobulinemia
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DOI: 10.3389/fimmu.2020.02001
Abstract: Background: X-linked agammaglobulinemia (XLA) is caused by a mutation of the Bruton's tyrosine kinase (BTK) gene and is the most common genetic mutation in patients with congenital agammaglobulinemia. The aim of this study was to… read more here.
Keywords: clinical features; pseudomonas sepsis; novel mutations; gene ... See more keywords