Pigmented Paravenous Chorioretinal Atrophy Is Associated with a Mutation within the Crumbs Homolog 1 (CRB1) Gene-Reference-Cited by-同舟云学术

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Pigmented Paravenous Chorioretinal Atrophy Is Associated with a Mutation within the Crumbs Homolog 1 (CRB1) Gene

Published:2005-01-01 Issue:1 Volume:46 Page:322
ISSN:1552-5783
Container-title:Investigative Opthalmology & Visual Science
language:en
Short-container-title:Invest. Ophthalmol. Vis. Sci.

Author:

McKay Gareth J.¹,Clarke Stephen¹,Davis Jason A.²,Simpson David A. C.¹,Silvestri Giuliana¹

Affiliation:

1. From the Ophthalmic Research Centre, Institute of Clinical Science, Queen’s University of Belfast, Belfast, Northern Ireland, United Kingdom; and the

2. Department of Biochemistry, University of Oxford, Oxford, United Kingdom.

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

Cited by 88 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. Pigmented paravenous retinochoroidal atrophy (PPRCA);Indian Journal of Ophthalmology - Case Reports;2024

2. Association of Circulating Antiretinal Antibodies With Clinical Outcomes in Retinitis Pigmentosa;Investigative Opthalmology & Visual Science;2023-12-13

3. New OCT and OCTA Insights in Inherited Retinal Dystrophies;Optical Coherence Tomography - Developments and Innovations in Ophthalmology;2023-09-06

4. Pigmented paravenous chorioretinal atrophy: Updated scenario;European Journal of Ophthalmology;2023-09-05

5. Case report: Familial foveal retinoschisis caused by CRB1 gene mutation in a family with recessive inheritance;Frontiers in Medicine;2023-08-11

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