Familial cases withMYH9disorders caused byMYH9S96L mutation
Author:
Publisher
Wiley
Subject
Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1442-200X.2012.03619.x/fullpdf
Reference11 articles.
1. Advances in the understanding of MYH9 disorders;Kunishima;Curr. Opin. Hematol.,2010
2. Hereditary macrothrombocytopenia, nephritis and deafness;Epstein;Am. J. Med.,1972
3. Expression of the nonmuscle myosin heavy chain IIA in the human kidney and screening for MYH9 mutations in Epstein and Fechtner syndrome;Arrondel;J. Am. Soc. Nephrol.,2001
4. Immunofluorescence analysis of neutrophil nonmuscle myosin heavy chain-A in MYH9 disorders: association of subcellular localization with MYH9 mutations;Kunishima;Lab. Invest.,2003
5. Renal manifestations of patients with MYH9-related disorders;Han;Pediatr. Nephrol.,2011
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. “MYH9 mutation and squamous cell cancer of the tongue in a young adult: a novel case report”;Diagnostic Pathology;2022-02-06
2. MYH9 disorder : Identification and a novel mutation in patients with macrothrombocytopenia;Pediatric Blood & Cancer;2021-04-15
3. A De Novo Mutation in MYH9 in a Child With Severe and Prolonged Macrothrombocytopenia;Journal of Pediatric Hematology/Oncology;2020-06-09
4. Management of patients with severe Epstein syndrome: Review of four patients who received living‐donor renal transplantation;Nephrology;2019-03-27
5. Whole exome sequencing in the diagnostic workup of patients with a bleeding diathesis;Haemophilia;2018-11-15
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
Copyright © 2019-2024 北京同舟云网络信息技术有限公司 京公网安备11010802033243号 京ICP备18003416号-3