A sensitive mutation screening strategy for Fabry disease: Detection of nine mutations in the α-galactosidase A gene
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference12 articles.
1. Human alpha-galactosidase A: nucleotide sequence of a cDNA clone encoding the mature enzyme.
2. Structural organization of the human alpha-galactosidase A gene: further evidence for the absence of a 3' untranslated region.
3. Mutation analysis in patients with the typical form of Anderson — Fabry disease
4. Mutation analysis in patients with the typical form of Anderson — Fabry disease
5. (1989) Fabry Disease: α-galactosidase deficiency; Schindler disease: α-N-acetylgalactosaminidase deficiency. In , , (eds): “The Metabolic Basis of Inherited Disease.” 6th Ed. New York: McGraw-Hill, pp 1751–1795.
Cited by 40 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. An Overview of Molecular Mechanisms in Fabry Disease;Biomolecules;2022-10-12
2. Fabry disease screening in high-risk populations in Japan: a nationwide study;Orphanet Journal of Rare Diseases;2020-08-26
3. Analysis of the alpha galactosidase gene: mutation profile and description of two novel mutations with extensive literature review in Turkish population;Journal of Pediatric Endocrinology and Metabolism;2020-08-19
4. Newborn screening for Fabry disease in the western region of Japan;Molecular Genetics and Metabolism Reports;2020-03
5. Future clinical and biochemical predictions of Fabry disease in females by methylation studies of the GLA gene;Molecular Genetics and Metabolism Reports;2019-09
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