Missense mutations in the DNA-binding region and termination codon in PAX6
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference35 articles.
1. Mutation in thePAX6 gene in twenty patients with aniridia
2. Haemoglobin Icaria, a new chain-termination mutant which causes α thalassaemia
3. Long range physical map of the Wilms' tumor-aniridia region on human chromosome 11
4. The 3′ untranslated region of messenger RNA: A molecular ‘hotspot’ for pathology?
Cited by 43 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 Analysis by NGS and MLPA in Chinese Aniridia Patients;2023-08-16
2. A rare case of congenital aniridia with an unusual run-on mutation in PAX6 gene;Indian Journal of Ophthalmology;2022
3. Genetics and epidemiology of aniridia: Updated guidelines for genetic study;Archivos de la Sociedad Española de Oftalmología (English Edition);2021-11
4. Genética y epidemiología de la aniridia congénita: actualización de buenas prácticas para el diagnóstico genético;Archivos de la Sociedad Española de Oftalmología;2021-11
5. Application of WES towards Molecular Investigation of Congenital Cataracts: Identification of Novel Alleles and Genes in a Hospital-Based Cohort of South India;International Journal of Molecular Sciences;2020-12-16
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