Compound Heterozygous Mutation of Rag1 Leading to Omenn Syndrome-Reference-Cited by-同舟云学术

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Compound Heterozygous Mutation of Rag1 Leading to Omenn Syndrome

Published:2015-04-07 Issue:4 Volume:10 Page:e0121489
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

Matthews Adam G. W.,Briggs Christine E.,Yamanaka Keiichi,Small Trudy N.,Mooster Jana L.,Bonilla Francisco A.,Oettinger Marjorie A.,Butte Manish J.

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference52 articles.

1. The mechanism and regulation of chromosomal V(D)J recombination;CH Bassing;Cell,2002

2. V(D)J recombination: RAG proteins, repair factors, and regulation;M Gellert;Annu Rev Biochem,2002

3. Non-homologous end-joining, a sticky affair;DC van Gent;Oncogene,2007

4. Familial Reticuloendotheliosis with Eosinophilia;GS Omenn;N Engl J Med,1965

5. Restricted heterogeneity of T lymphocytes in combined immunodeficiency with hypereosinophilia (Omenn's syndrome);G de Saint-Basile;J Clin Invest,1991

Cited by 10 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Heterogeneity in RAG1 and RAG2 deficiency: 35 cases from a single-centre;Clinical and Experimental Immunology;2023-09-19

2. V(D)J Recombination: Recent Insights in Formation of the Recombinase Complex and Recruitment of DNA Repair Machinery;Frontiers in Cell and Developmental Biology;2022-04-29

3. A Girl with Erythema all Over the Body;Clinical Cases in Pediatric Skin Cancers;2022

4. Diagnostic Yield and Therapeutic Consequences of Targeted Next-Generation Sequencing in Sporadic Primary Immunodeficiency;International Archives of Allergy and Immunology;2021-10-07

5. Erythroderma in a newborn infant suggesting Omenn syndrome;British Journal of Dermatology;2020-05-12

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