Analysis of Clinical Presentations of Bruton Disease: A Review of 20 Years of Accumulated Data from Pediatric Patients at Severance Hospital

PURPOSE: X-linked agammaglobulinemia (XLA) is a humoral immunodeficiency disease caused by a mutation in the Bruton tyrosine kinase (BTK) gene resulting in defective B cell differentiation. Because it is a relatively rare disorder, it is difficult for clinicians to have a comprehensive understanding...

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Detalles Bibliográficos
Autores principales: Chun, Jin-Kyong, Lee, Taek Jin, Song, Jae Woo, Linton, John A, Kim, Dong Soo
Formato: Texto
Lenguaje:English
Publicado: Yonsei University College of Medicine 2008
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2615253/
https://www.ncbi.nlm.nih.gov/pubmed/18306466
http://dx.doi.org/10.3349/ymj.2008.49.1.28

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2615253/
https://www.ncbi.nlm.nih.gov/pubmed/18306466
http://dx.doi.org/10.3349/ymj.2008.49.1.28

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