Progressive increase in FIX level in males with haemophilia B Leyden and c.35G > A mutation in early childhood not related to androgen effect
Author:
Affiliation:
1. Our Lady's Hospital Crumlin Dublin Ireland
2. Saint James's Hospital Dublin Ireland
Publisher
Wiley
Subject
Hematology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/bjh.16688
Reference16 articles.
1. Hemophilia B: molecular pathogenesis and mutation analysis
2. The Hemophilias — From Royal Genes to Gene Therapy
3. Hemophilia B Leyden
4. The putative factor IX gene promoter in hemophilia B Leyden
5. Another Genetic Variant of Haemophilia B: Haemophilia B Leyden
Cited by 7 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. Genotype-phenotype analyses of Iranian patients with hemophilia B (Leyden -) and hemophilia B (Leyden +): A single-center study;Transfusion and Apheresis Science;2024-08
2. Genotype-phenotype analyses of Iranian patients with and without hemophilia B Leyden: A single-center study;2024-03-18
3. An updated interactive database for 1692 genetic variants in coagulation factor IX provides detailed insights into hemophilia B;Journal of Thrombosis and Haemostasis;2023-05
4. The Molecular Basis of FIX Deficiency in Hemophilia B;International Journal of Molecular Sciences;2022-03-02
5. The Clinical Genetics of Hemophilia B (Factor IX Deficiency);The Application of Clinical Genetics;2021-11
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