Origin of mutation in sporadic cases of haemophilia-B
Author:
Publisher
Wiley
Subject
Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.1992.tb00585.x/fullpdf
Reference19 articles.
1. The gene structure of human antihaemophilic factor IX;Anson;EMBO J,1984
2. Nucleotide sequence of the gene for human factor IX (antihaemophilia B);Yoshitake;Biochemistry,1985
3. Diagnostic symptoms of severe and moderate haemophilia A and B;Ljung;Acta Paediat Scand,1990
4. Reactivity of cytosine and thymine in single-base-pair mismatches with hydroxylamaine and osmium tetroxide and its application to the study of mutations;Cotton;Proc Natl Acad Sci USA,1988
5. Direct detection of point mutations by mismatch analysis: application to haemopbilia B;Montandon;Nucl Acids Res,1989
Cited by 14 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. Origin of pathogenic variant and mosaicism in families with a sporadic case of haemophilia B;Haemophilia;2024-04-17
2. Hemophilia B — Mutation Rates and Incidence — A Simulation Study;Twin Research and Human Genetics;2020-06
3. Recommendations for the clinical interpretation of genetic variants and presentation of results to patients with inherited bleeding disorders. A UK Haemophilia Centre Doctors’ Organisation Good Practice Paper;Haemophilia;2019-01
4. Genetics 101: understanding transmission and genetic testing of inherited bleeding disorders;The Journal of Haemophilia Practice;2019-01-01
5. Factor VIII therapy for hemophilia A: current and future issues;Expert Review of Hematology;2014-04-10
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