OTX2 mutation associated with severe myopia in a Canadian family-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

OTX2 mutation associated with severe myopia in a Canadian family

Published:2021-12-26 Issue: Volume: Page:1-3
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Wangding Snow¹^ORCID,Colaiacovo Samantha²,Makar Inas¹³,Saleh Maha¹²

Affiliation:

1. Department of Pediatrics, Schulich School of Medicine and Dentistry, London, Canada

2. Division of Medical Genetics, Department of Pediatrics, London Health Sciences Centre, London, Canada

3. Department of Ophthalmology, St. Joseph’s Hospital, London, Canada

Funder

funding

Publisher

Informa UK Limited

Subject

Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/13816810.2021.2015791

Reference12 articles.

1. Novel heterozygousOTX2mutations and whole gene deletions in anophthalmia, microphthalmia and coloboma

2. OTX2 Activates the Molecular Network Underlying Retina Pigment Epithelium Differentiation

3. OTX2mutations contribute to the otocephaly-dysgnathia complex

4. Heterozygous Mutations of OTX2 Cause Severe Ocular Malformations

Cited by 1 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. Non-syndromic OTX2-associated pattern dystrophy: a 10-year multimodal imaging study;Documenta Ophthalmologica;2024-07-18

同舟云学术

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