Clinical, Molecular, Immunological Properties and Our Clinical Experiences in Patients Diagnosed with X-linked Agamaglobulinemia

Objective: As a primary immunodeficiency X-linked agammaglobulinemia (XLA) that develops due to Bruton tyrosine kinase signal transduction protein deficiency which progresses with antibody deficiency was firstly described by an American pediatrician Ogden Bruton. In our study, we have aimed to evalu...

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Bibliographic Details

Published in:	Journal of Behçet Uz Children's Hospital
Main Authors:	Ezgi Balkarlı, Selime Özen Bölük, Ömer Akçal, İlke Taşkırdı, İdil Akay Haci, Nesrin Gülez, Ferah Genel
Format:	Article
Language:	English
Published:	Izmir Dr. Behcet Uz Children’s Hospital 2023-12-01
Subjects:	x-linked agammaglobulinemia bruton tyrosine kinase primary immunodeficiencies
Online Access:	https://jag.journalagent.com/z4/download_fulltext.asp?pdir=behcetuz&un=BUCHD-78545