Identification of three novel mutations in Japanese patients with Menkes disease and mutation screening by denaturing high performance liquid chromatography
Author:
Publisher
Wiley
Subject
Pediatrics, Perinatology and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1442-200x.2004.02012.x/fullpdf
Reference13 articles.
1. Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein
2. Isolation of a partial candidate gene for Menkes disease by positional cloning
3. Isolation of a candidate gene for Menkes disease and evidence that it encodes a copper–transporting ATPase
4. Screening of 383 unrelated patients affected with Menkes disease and finding of 57 gross deletions inATP7A
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. ATP7A Clinical Genetics Resource – A comprehensive clinically annotated database and resource for genetic variants in ATP7A gene;Computational and Structural Biotechnology Journal;2020
2. A Case of Menkes Disease First Manifested as Severe Vesicoureteral Reflux Caused by a Novel Mutation in ATP7A Gene;Journal of the korean child neurology society;2017-12
3. An Overview and Update ofATP7AMutations Leading to Menkes Disease and Occipital Horn Syndrome;Human Mutation;2013-03
4. Splice Site Mutations in the ATP7A Gene;PLoS ONE;2011-04-11
5. Molecular diagnosis of Menkes disease: Genotype–phenotype correlation;Biochimie;2009-10
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