Autofluorescence Imaging and Spectral-Domain Optical Coherence Tomography in Incomplete Congenital Stationary Night Blindness and Comparison With Retinitis Pigmentosa-Reference-Cited by-同舟云学术

Autofluorescence Imaging and Spectral-Domain Optical Coherence Tomography in Incomplete Congenital Stationary Night Blindness and Comparison With Retinitis Pigmentosa

Published:2012-01 Issue:1 Volume:153 Page:143-154.e2
ISSN:0002-9394
Container-title:American Journal of Ophthalmology
language:en
Short-container-title:American Journal of Ophthalmology

Author:

Chen Royce W.S.,Greenberg Jonathan P.,Lazow Margot A.,Ramachandran Rithu,Lima Luiz H.,Hwang John C.,Schubert Carl,Braunstein Alexandra,Allikmets Rando,Tsang Stephen H.

Funder

National Eye Institute, National Institutes of Health

Department of Defense

Publisher

Elsevier BV

Subject

Ophthalmology

Reference30 articles.

1. Congenital stationary night blindness with negative electroretinogram: a new classification;Miyake;Arch Ophthalmol,1986

2. Novel CACNA1F mutations in Japanese patients with incomplete congenital stationary night blindness;Nakamura;Invest Ophthalmol Vis Sci,2001

3. Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness;Bech-Hansen;Nat Genet,2000

4. An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness;Strom;Nat Genet,1998

5. Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness;Bech-Hansen;Nat Genet,1998

Cited by 34 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. Night blindness in a man with a normal fundus examination;Clinical Cases in Medical Retina;2025

2. Congenital Stationary Night Blindness;Ophthalmology Retina;2024-09

3. Multimodal imaging in Schubert-Bornschein congenital stationary night blindness;Ophthalmic Genetics;2022-10-13

4. Approach to inherited retinal diseases;Indian Journal of Ophthalmology;2022

5. Congenital Stationary Night Blindness;Inherited Retinal Disease;2022