Autosomal Dominant Occult Macular Dystrophy with an RP1L1 Mutation (R45W)-Reference-Cited by-同舟云学术

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Autosomal Dominant Occult Macular Dystrophy with an RP1L1 Mutation (R45W)

Published:2012-05 Issue:5 Volume:89 Page:684-691
ISSN:1040-5488
Container-title:Optometry and Vision Science
language:en
Short-container-title:

Author:

Hayashi Takaaki,Gekka Tamaki,Kozaki Kenichi,Ohkuma Yasuhiro,Tanaka Isako,Yamada Hisashi,Tsuneoka Hiroshi

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Optometry,Ophthalmology

Reference21 articles.

1. Hereditary macular dystrophy without visible fundus abnormality.;Miyake;Am J Ophthalmol,1989

2. Occult macular dystrophy.;Miyake;Am J Ophthalmol,1996

3. Multifocal electroretinogram in occult macular dystrophy.;Piao;Invest Ophthalmol Vis Sci,2000

4. Non-familial occult macular dystrophy.;Lyons;Doc Ophthalmol,2005

5. Foveal thickness in occult macular dystrophy.;Kondo;Am J Ophthalmol,2003

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1. A mild form of POC1B-associated retinal dystrophy with relatively preserved cone system function;Documenta Ophthalmologica;2023-05-25

2. Occult Macular Dystrophy: a case report and major review;Ophthalmic Genetics;2022-06-29

3. RP1L1 rs3924612 gene polymorphism and RP1L1 protein associations among patients with early age-related macular degeneration;Ophthalmic Genetics;2021-12-05

4. Spatial Functional Characteristics of East Asian Patients With Occult Macular Dystrophy (Miyake Disease); EAOMD Report No. 2;American Journal of Ophthalmology;2021-01

5. RP1L1 and inherited photoreceptor disease: A review;Survey of Ophthalmology;2020-11

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