Clinical, Molecular, Immunological Properties and Our Clinical Experiences in Patients Diagnosed with X-linked Agamaglobulinemia
Author:
Publisher
Galenos Yayinevi
Subject
General Medicine
Reference31 articles.
1. 1. Tsukada S, Saffran DC, Rawlings DJ, Parolini O, Allen RC, Klisak I, et al. Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemia. Cell. 1993;72(2):279-90. doi: 10.1016/0092-8674(93)90667-f.
2. 2. Vetrie D, Vorechovský I, Sideras P, Holland J, Davies A, Flinter F, et al. The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases. Nature. 1993;361(6409):226-33. doi: 10.1038/361226a0.
3. 3. Vihinen M, Kwan SP, Lester T, Ochs HD, Resnick I, Väliaho J, et al. Mutations of the human BTK gene coding for bruton tyrosine kinase in X-linked agammaglobulinemia. Hum Mutat. 1999;13(4):280-5. doi: 10.1002/(SICI)1098-1004(1999)13:4<280::AID-HUMU3>3.0.CO;2-L.
4. 4. Suri D, Rawat A, Singh S. X-linked Agammaglobulinemia. Indian J Pediatr. 2016;83(4):331-7. doi: 10.1007/s12098-015-2024-8.
5. 5. Sideras P, Müller S, Shiels H, Jin H, Khan WN, Nilsson L, et al. Genomic organization of mouse and human Bruton's agammaglobulinemia tyrosine kinase (Btk) loci. J Immunol. 1994;153(12):5607-17. doi: 10.4049/jimmunol.153.12.5607.
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