Potential pathogenic mechanism of type 1 X-linked lymphoproliferative syndrome caused by a mutation of SH2D1A gene in an infant: A case report-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Potential pathogenic mechanism of type 1 X-linked lymphoproliferative syndrome caused by a mutation of SH2D1A gene in an infant: A case report

Published:2022-10-14 Issue:41 Volume:101 Page:e30951
ISSN:1536-5964
Container-title:Medicine
language:en
Short-container-title:

Author:

Wang Yanchun,Wang Yan,Lu Weimin,Tao Lvyan,Xiao Yang,Zhou Yuantao,He Xiaoli,Zhang Yu,Li Li

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

General Medicine

Reference30 articles.

1. X-linked recessive progressive combined variable immunodeficiency (Duncan’s disease).;Purtilo;Lancet (London, England),1975

2. Correlation of mutations of the SH2D1A gene and Epstein-Barr virus infection with clinical phenotype and outcome in X-linked lymphoproliferative disease.;Sumegi;Blood,2000

3. Host response to EBV infection in X-linked lymphoproliferative disease results from mutations in an SH2-domain encoding gene.;Coffey;Nat Genet,1998

4. XIAP deficiency in humans causes an X-linked lymphoproliferative syndrome.;Rigaud;Nature,2006

5. X-linked lymphoproliferative syndromes: brothers or distant cousins?;Filipovich;Blood,2010

Cited by 1 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. Association of sh2 domain-containing protein 1a, immunoglobulins and T lymphocyte subsets with epstein- barr virus infections;The Turkish Journal of Pediatrics;2023

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP