PAX6 Genotypic and Retinal Phenotypic Characterization in Congenital Aniridia-Reference-Cited by-同舟云学术

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PAX6 Genotypic and Retinal Phenotypic Characterization in Congenital Aniridia

Published:2020-05-12 Issue:5 Volume:61 Page:14
ISSN:1552-5783
Container-title:Investigative Opthalmology & Visual Science
language:en
Short-container-title:Invest. Ophthalmol. Vis. Sci.

Author:

Pedersen Hilde R.¹,Baraas Rigmor C.¹,Landsend Erlend C. S.²,Utheim Øygunn A.²,Utheim Tor P.¹,Gilson Stuart J.¹,Neitz Maureen³

Affiliation:

1. National Centre for Optics, Vision and Eye Care, Faculty of Health and Social Sciences, University of South-Eastern Norway, Kongsberg, Norway

2. Department of Ophthalmology, Oslo University Hospital, Oslo, Norway

3. Department of Ophthalmology, University of Washington, Seattle, Washington, United States

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

Cited by 31 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. Analysis of Phenotypes Associated with Deficiency of PAX6 Haplotypes in Chinese Aniridia Families;Current Medical Science;2024-07-05

2. Multimodal in-vivo maps as a tool to characterize retinal structural biomarkers for progression in adult-onset Stargardt disease;Frontiers in Ophthalmology;2024-04-23

3. A rare missense PAX6 mutation causes atypical aniridia in a three-generation Chinese family;International Journal of Ophthalmology;2024-03-18

4. Multi-omics analysis in human retina uncovers ultraconserved cis-regulatory elements at rare eye disease loci;Nature Communications;2024-02-21

5. Optic Disc Hypoplasia Assessment in PAX6-Related Aniridia;Journal of Neuro-Ophthalmology;2024-01-16

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