Mutation in the TCRα subunit constant gene (TRAC) leads to a human immunodeficiency disorder characterized by a lack of TCRαβ+ T cells-Reference-Cited by-同舟云学术

Mutation in the TCRα subunit constant gene (TRAC) leads to a human immunodeficiency disorder characterized by a lack of TCRαβ+ T cells

Published:2011-02-01 Issue:2 Volume:121 Page:695-702
ISSN:0021-9738
Container-title:Journal of Clinical Investigation
language:en
Short-container-title:J. Clin. Invest.

Author:

Morgan Neil V.,Goddard Sarah,Cardno Tony S.,McDonald David,Rahman Fatimah,Barge Dawn,Ciupek Andrew,Straatman-Iwanowska Anna,Pasha Shanaz,Guckian Mary,Anderson Graham,Huissoon Aarnoud,Cant Andrew,Tate Warren P.,Hambleton Sophie,Maher Eamonn R.

Publisher

American Society for Clinical Investigation

Subject

General Medicine

Reference24 articles.

1. Human Primary Immunodeficiency Diseases

2. Unravelling the association of partial T-cell immunodeficiency and immune dysregulation

3. Translational termination efficiency in mammals is influenced by the base following the stop codon.

4. Comparison of characteristics and function of translation termination signals between and within prokaryotic and eukaryotic organisms

5. Importance of the T cell receptor α-chain transmembrane distal region for assembly with cognate subunits

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