Homozygous mutations in LPIN2 are responsible for the syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anaemia (Majeed syndrome)-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Homozygous mutations in LPIN2 are responsible for the syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anaemia (Majeed syndrome)

Published:2005-07-01 Issue:7 Volume:42 Page:551-557
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Ferguson P J

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Cited by 350 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. Bacterial infections of the bones and joints;Remington and Klein's Infectious Diseases of the Fetus and Newborn Infant;2025

2. Architecture and function of yeast phosphatidate phosphatase Pah1 domains/regions;Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids;2024-12

3. Chronic Noninfectious Osteomyelitis: A Review of Imaging Findings;Indian Journal of Radiology and Imaging;2024-09-03

4. Inflammatory turmoil within: an exploration of autoinflammatory disease genetic underpinnings, clinical presentations, and therapeutic approaches;Advances in Rheumatology;2024-08-22

5. Simultaneous onset of chronic nonbacterial osteomyelitis in siblings;Modern Rheumatology Case Reports;2024-08-03

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