Oguchi disease masked by retinitis pigmentosa

Author:

Sonoyama Hiroko,Shinoda Kei,Ishigami Chie,Tada Yumi,Ideta Hidenao,Ideta Ryuichi,Takahashi Masayo,Miyake Yozo

Publisher

Springer Science and Business Media LLC

Subject

Physiology (medical),Sensory Systems,Ophthalmology

Reference20 articles.

1. Oguchi C (1907) On a type of night-blindness. Acta Soc Ophthalmol Jpn 11:123–134 (Japanese)

2. Miyake Y (2006) Oguchi’s disease. In: Miyake Y (ed) Electrodiagnosis of retinal diseases. Springer, Tokyo, pp 119–122

3. Miyake Y, Horiguchi M, Suzuki S, Kondo M, Tanikawa A (1996) Electrophysiological findings in patients with Oguchi’s disease. Jpn J Ophthalmol 40:511–519

4. Fuchs S, Nakazawa M, Maw M, Tamai M, Oguchi Y, Gal A (1995) A homozygous 1-base pair deletion in the arrestin gene is a frequent cause of Oguchi disease in Japanese. Nat Genet 10:360–362

5. Yamamoto S, Sippel KC, Berson EL, Dryja TP (1997) Defects in the rhodopsin kinase gene in the Oguchi form of stationary night blindness. Nat Genet 15:175–178

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1. Genetic analysis and clinical features of three Chinese patients with Oguchi disease;Documenta Ophthalmologica;2022-11-22

2. A compound heterozygous mutation in the S-Antigen Visual Arrestin SAG gene in a Chinese patient with Oguchi type one: a case report;BMC Ophthalmology;2022-03-04

3. Genetic dissection of non-syndromic retinitis pigmentosa;Indian Journal of Ophthalmology;2022

4. Retinitis Pigmentosa and Allied Diseases;Albert and Jakobiec's Principles and Practice of Ophthalmology;2022

5. Retinitis Pigmentosa and Allied Diseases;Albert and Jakobiec's Principles and Practice of Ophthalmology;2021-09-25

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