Molecular genetic testing for familial hypercholesterolemia: spectrum of LDL receptor gene mutations in the Netherlands-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Molecular genetic testing for familial hypercholesterolemia: spectrum of LDL receptor gene mutations in the Netherlands

Published:2000-02 Issue:2 Volume:57 Page:116-124
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clinical Genetics

Author:

Lombardi M Paola,Redeker Egbert Jw,Defesche Joep C,Kamerling Sylvia Wa,Trip Mieke D,Mannens Marcel Mam,Havekes Louis M,Kastelein John Jp

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-0004.2000.570205.x/fullpdf

Reference44 articles.

1. Familial Defective Apolipoprotein B-100 Is Clinically Indistinguishable From Familial Hypercholesterolemia

2. A Third Major Locus for Autosomal Dominant Hypercholesterolemia Maps to 1p34.1-p32

3. Molecular genetics of the LDL receptor gene in familial hypercholesterolemia

4. LDLR Database (second edition): new additions to the database and the software, and results of the first molecular analysis

Cited by 42 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. Genetic testing for familial hypercholesterolemia—past, present, and future;Journal of Lipid Research;2021

2. PCSK9 Inhibitors in a Statin-Intolerant Transgender Man With Heterozygous Familial Hypercholesterolemia: A Case Report;Journal of the Endocrine Society;2019-06-06

3. Prevalence, Identification, and Scouting for Familial Hypercholesterolaemia Including Registries;Current Pharmaceutical Design;2019-01-02

4. Achieved LDL cholesterol levels in patients with heterozygous familial hypercholesterolemia: A model that explores the efficacy of conventional and novel lipid-lowering therapy;Journal of Clinical Lipidology;2018-07

5. Selection of individuals for genetic testing for familial hypercholesterolaemia: development and external validation of a prediction model for the presence of a mutation causing familial hypercholesterolaemia;European Heart Journal;2016-04-03

同舟云学术

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