Clinical Characteristics and Molecular Analysis of 21 Chinese Children with Congenital Agammaglobulinemia-Reference-Cited by-同舟云学术

Clinical Characteristics and Molecular Analysis of 21 Chinese Children with Congenital Agammaglobulinemia

Published:2010-10-05 Issue:5 Volume:72 Page:454-459
ISSN:0300-9475
Container-title:Scandinavian Journal of Immunology
language:en
Short-container-title:

Author:

Zhang Z.-Y.,Zhao X.-D.,Jiang L.-P.,Liu E.-M.,Wang M.,Yu J.,Liu P.,Yang X.-Q.

Publisher

Wiley

Subject

Immunology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-3083.2010.02457.x/fullpdf

Reference24 articles.

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2. Genetic defect in human X-linked agammaglobulinemia impedes a maturational evolution of pro-B cells into a later stage of pre-B cells in the B-cell differentiation pathway;Nomura;Blood,2000

3. Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemia;Tsukada;Cell,1993

4. The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases;Vetrie;Nature,1993

5. Genomic organization and structure of Bruton agammaglobulinemia tyrosine kinase: localization of mutations associated with varied clinical presentations and course in X chromosome-linked agammaglobulinemia;Ohta;Proc Natl Acad Sci U S,1994

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