A common 253-kb deletion involving VWF and TMEM16B in German and Italian patients with severe von Willebrand disease type 3
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1538-7836.2007.02460.x/fullpdf
Reference23 articles.
1. BIOCHEMISTRY AND GENETICS OF VON WILLEBRAND FACTOR
2. Gene conversions are a common cause of von Willebrand disease
3. Genetic heterogeneity of severe von Willebrand disease type III in the German population
4. Characterization of Partial Gene Deletions in Type III von Willebrand Disease with Alloantibody Inhibitors
5. Severe type III von Willebrand's disease caused by deletion of exon 42 of the von Willebrand factor gene: family studies that identify carriers of the condition and a compound heterozygous individual
Cited by 39 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. Emicizumab in Type 3 von Willebrand Disease: Report of a Case with an Alloantibody and Literature Review;Seminars in Thrombosis and Hemostasis;2024-06-27
2. Genotyping R1336X and Eliminating the Pseudogene Amplification in Type 3 von Willebrand Disease Patients;Indian Journal of Hematology and Blood Transfusion;2024-06-24
3. The physiological roles of anoctamin2/TMEM16B and anoctamin1/TMEM16A in chemical senses;Cell Calcium;2024-06
4. Genotypes of European and Iranian patients with type 3 von Willebrand disease enrolled in 3WINTERS-IPS;Blood Advances;2021-08-05
5. Rapid host response to an infection with Coronavirus. Study of transcriptional responses with Porcine Epidemic Diarrhea Virus;2020-07-28
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