BTKbase: XLA-mutation registry
Author
Summary, in English
X-linked agammaglobulinemia (XLA) is an immunodeficiency caused by mutations in the gene coding for Bruton's agammaglobulinemia tyrosine kinase (Btk). A new edition of the database (BTKbase) of Btk mutations has been compiled containing 282 patient entries representing 175 unique molecular events.
Publishing year
1996
Language
English
Pages
502-506
Publication/Series
Immunology Today
Volume
17
Issue
11
Document type
Journal article
Publisher
Elsevier
Topic
- Medical Genetics
Status
Published
ISBN/ISSN/Other
- ISSN: 0167-5699