Analysis of Btk Mutations in Patients with X-Linked Agammaglobulinaemia (XLA) and Determination of Carrier Status in Normal Female Relatives: a Nationwide Study of Btk Deficiency in Greece-Reference-Cited by-同舟云学术

Analysis of Btk Mutations in Patients with X-Linked Agammaglobulinaemia (XLA) and Determination of Carrier Status in Normal Female Relatives: a Nationwide Study of Btk Deficiency in Greece

Published:2001-09 Issue:3 Volume:54 Page:321-327
ISSN:0300-9475
Container-title:Scandinavian Journal of Immunology
language:en
Short-container-title:

Author:

Speletas M.,Kanariou M.,Kanakoudi-Tsakalidou F.,Papadopoulou-Alataki E.,Arvanitidis K.,Pardali E.,Constantopoulos A.,Kartalis G.,Vihinen M.,Sideras P.,Ritis K.

Publisher

Wiley

Subject

Immunology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-3083.2001.00967.x/fullpdf

Reference44 articles.

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2. Molecular basis for three X-linked immune disorders;Puck;Hum Mol Gen,1994

3. The Bruton's tyrosine kinase gene is expressed throughout B-cell differentiation, from early B cell stages preceding immunoglobulin gene rearrangement up to mature B cell stages;De Weers;Eur J Immunol,1993

4. X-linked agammaglobulinemia;Goddpard;S Afr Med J,1989

5. X-linked agammaglobulinemia. A clinical and molecular analysis;Ochs;Medicine,1996

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