Mutation-Specific PCR: A Rapid and Inexpensive Diagnostic Method, as Exemplified by Mitochondrial DNA Analysis in Leber's Hereditary Optic Neuropathy
Author:
Publisher
Mary Ann Liebert Inc
Subject
Cell Biology,Genetics,Molecular Biology,General Medicine
Link
http://www.liebertpub.com/doi/pdf/10.1089/dna.1993.12.549
Reference16 articles.
1. Sequence and organization of the human mitochondrial genome
2. Technical aspects of typing for HLA-DP alleles using allele-specific DNA in vitro amplification and sequence-specific oligonucleotide probes
3. Improved Molecular-Genetic Diagnosis of Leber's Hereditary Optic Neuropathy
4. Analysis of any point mutation in DNA. The amplification refractory mutation system (ARMS)
Cited by 4 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. Screening for mutations of the cationic trypsinogen gene: are they of relevance in chronic alcoholic pancreatitis?;Gut;1999-03-01
2. Development of reverse dot-blot system for screening of mitochondrial DNA mutations associated with Leber hereditary optic atrophy;Clinical Chemistry;1997-01-01
3. Molecular biology techniques;Analytical Chemistry;1995-06-15
4. Leber's hereditary optic neuropathy associated with a disorder indistinguishable from multiple sclerosis in a male harbouring the mitochondrial DNA 11778 mutation;Acta Neurologica Scandinavica;1995-05
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