BTKbase, mutation database for X-linked agammaglobulinemia (XLA)-Reference-Cited by-同舟云学术

BTKbase, mutation database for X-linked agammaglobulinemia (XLA)

Published:1997-01-01 Issue:1 Volume:25 Page:166-171
ISSN:0305-1048
Container-title:Nucleic Acids Research
language:en
Short-container-title:Nucleic Acids Research

Author:

Vihinen M.,Belohradsky B. H.,Haire R. N.,Holinski-Feder E.,Kwan S.-P.,Lappalainen I.,Lehvaslaiho H.,Lester T.,Meindl A.,Ochs H. D.,Ollila J.,Vorechovsky I.,Weiss M.,Smith C. I. E.

Publisher

Oxford University Press (OUP)

Subject

Genetics

Link

http://academic.oup.com/nar/article-pdf/25/1/166/3791116/25-1-166.pdf

Reference52 articles.

1. The gene involved in X-linked agammaglobulinaemia is a member of the src family of protein-tyrosine kinases

2. Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemia

3. Molecular and Cellular Aspects of X-Linked Agammaglobulinemia

4. Mapping of the X-linked agammaglobulinemia locus by use of restriction fragment-length polymorphism.

5. Heterogeneity in the map distance between X-linked agammaglobulinemia and a map of nine RFLP loci

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