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

• Autors principals: Ezgi Balkarlı (Autor), Selime Özen Bölük (Autor), Ömer Akçal (Autor), İlke Taşkırdı (Autor), İdil Akay Haci (Autor), Nesrin Gülez (Autor), Ferah Genel (Autor)
• Format: Llibre
• Publicat: Galenos Publishing House, 2023-12-01T00:00:00Z.
• Matèries: article
• Accés en línia: Connect to this object online.

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...