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Nov 11, 2019 - Purpose: X-linked agammaglobulinemia (XLA) is a humoral immunodeficiency disease caused by a mutation in the Bruton tyrosine kinase (BTK) gene resulting Korean X-Linked Agammaglobulinemia. Bruton's Tyrosine Kinase Gene from Seven in. Novel Regulatory Defect in the First Intron,. Characterization of Mutations Feb 15, 2017 - This information is current as. Immunodeficiency. Agammaglobulinemia, the First Primary. Molecular Basis of X-Linked. Colonel Bruton's Kinase Defined the. We present a 22-month-old boy with X-linked agammaglobulinemia masked by normal immunoglobulin a novel Bruton tyrosine kinase gene mutation. He was May 14, 2015 - X-Linked Agammaglobulinemia (XLA) was first described in 1952 by Dr. Ogden Bruton. This disease, sometimes called Bruton's Agammaglobulinemia or. Feb 23, 2018 - Feb 23, 2018 -