Molecular and Structural Characterization of Five Novel Mutations in the Bruton’s Tyrosine Kinase Gene from Patients with X-Linked Agammaglobulinemia-Reference-Cited by-同舟云学术

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Molecular and Structural Characterization of Five Novel Mutations in the Bruton’s Tyrosine Kinase Gene from Patients with X-Linked Agammaglobulinemia

Published:1997-07 Issue:7 Volume:3 Page:477-485
ISSN:1076-1551
Container-title:Molecular Medicine
language:en
Short-container-title:Mol Med

Author:

Saha Bratin K.,Curtis Sherill K.,Vogler Larry B.,Vihinen Mauno

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics,Molecular Biology,Molecular Medicine

Link

http://link.springer.com/content/pdf/10.1007/BF03401694.pdf

Reference43 articles.

1. Bruton OC (1952) Agammaglobulinemia. Pediatrics 9: 722–728.

2. Kornfeld SJ, Haire RN, Strong SJ, et al (1996) A novel mutation (Cys145 to stop) in Bruton’s tyrosine kinase is associated with newly diagnosed X-linked agammaglobulinemia in a 51-year-old male. Mol Med. 2: 619–623.

3. Buckley RH (1994) Assessing inheritance of agammaglobulinemia. New Engl J. Med. 330: 1526–1528.

4. Tsukada S, Saffran DC, Rawlings DJ, et al. (1993) Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemia. Cell 72: 279–290.

5. Vetrie D, Vorechovsky I, Sideras P, et al. (1993) The gene involved in X-linked agammaglobulinaemia is a member of the SRC family of protein-tyrosine kinases. Nature (Lond.) 361: 226–233.

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