A hypomorphic recombination-activating gene 1 (RAG1) mutation resulting in a phenotype resembling common variable immunodeficiency-Reference-Cited by-同舟云学术

A hypomorphic recombination-activating gene 1 (RAG1) mutation resulting in a phenotype resembling common variable immunodeficiency

Published:2014-12 Issue:6 Volume:134 Page:1375-1380
ISSN:0091-6749
Container-title:Journal of Allergy and Clinical Immunology
language:en
Short-container-title:Journal of Allergy and Clinical Immunology

Author:

Abolhassani Hassan,Wang Ning,Aghamohammadi Asghar,Rezaei Nima,Lee Yu Nee,Frugoni Francesco,Notarangelo Luigi D.,Pan-Hammarström Qiang,Hammarström Lennart

Publisher

Elsevier BV

Subject

Immunology,Immunology and Allergy

Reference43 articles.

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3. Leaky severe combined immunodeficiency and aberrant DNA rearrangements due to a hypomorphic RAG1 mutation;Giblin;Blood,2009

4. Mutational analysis of all conserved basic amino acids in RAG-1 reveals catalytic, step arrest, and joining-deficient mutants in the V(D)J recombinase;Huye;Mol Cell Biol,2002

5. Intermediates in V(D)J recombination: a stable RAG1/2 complex sequesters cleaved RSS ends;Jones;Proc Natl Acad Sci U S A,2001

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