Factor VIII gene rearrangements in patients with severe haemophilia A
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference7 articles.
1. Report of a joint WHO/WFH meeting on the control of haemophilia: carrier detection and prenatal diagnosis;Peake;Blood Coag Fibrin,1993
2. Molecular characterisation of severe haemophilia A suggests that about half the mutations are not within the coding regions and splice junctions of the factor VIII gene;Higuchi;Proc Natl Acad Sci USA,1991
3. Analysis of factor VIII mRNA reveals defects in everyone of 28 haemophilia A patients;Naylor;Hum Molec Genet,1993
4. Characteristic mRNA abnormality found in half the patients with severe haemophilia A is due to large DNA inversions;Naylor;Hum Molec Genet,1993
5. Inversions disrupting the factor VIII gene as a common cause of severe haemophilia A;Lakich;Nature Genet,1993
Cited by 54 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 Bleeding Tendency and Arthropathy Development in Individuals with Hemophilia;Seminars in Thrombosis and Hemostasis;2021-02-26
2. High resolution melting for F9 gene mutation analysis in patients with haemophilia B;BLOOD TRANSFUS-ITALY;2019
3. Accurate, simple, and inexpensive assays to diagnose F8 gene inversion mutations in hemophilia A patients and carriers;Blood Advances;2016-12-14
4. Phenotypic Heterogeneity of Hemostasis in Severe Hemophilia;Seminars in Thrombosis and Hemostasis;2015-01-23
5. Detection of Hemophilia A Carriers in Azeri Turkish Population of Iran;Clinical and Applied Thrombosis/Hemostasis;2014-03-25
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