Recent advances in genetic analyses of oculocutaneous albinism types 2 and 4
Author:
Publisher
Elsevier BV
Subject
Dermatology,Molecular Biology,Biochemistry
Reference45 articles.
1. Human oculocutaneous albinism caused by a single base insertion in the tyrosinase gene;Tomita;Biochem Biophy Res Commun,1989
2. Genetics of pigmentary disorders;Tomita;Am J Med Genet,2004
3. Molecular genetics of oculocutaneous albinism;Spritz;Hum Mol Genet,1994
4. Hermansky–Pudlak syndrome and pale ear: melanosome-making for the millennium;Spritz;Pigment Cell Res,2000
5. Molecular basis of albinism: mutations and polymorphisms of pigmentation genes associated with albinism;Oetting;Hum Mutat,1999
Cited by 92 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 of albinism caused by compound heterozygous mutations of the OCA2 gene in a Chinese family;Hereditas;2024-02-06
2. Oculocutaneous albinism type 4: Novel compound heterozygous mutations in the SLC45A2 gene in a Chinese case;Molecular Genetics & Genomic Medicine;2024-02
3. The Slc45a4 Gene Regulates Pigmentation in a Manner Distinct from that of the OCA4 Gene Slc45a2;Journal of Investigative Dermatology;2023-09
4. OCA7 is a melanosome membrane protein that defines pigmentation by regulating early stages of melanosome biogenesis;Journal of Biological Chemistry;2022-12
5. Causal gene identification and desirable trait recreation in goldfish;Science China Life Sciences;2022-11-10
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