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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| Main Authors: | , , , , , , |
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| Format: | Book |
| Published: |
Galenos Publishing House,
2023-12-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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