2Usui T, Iehibe M, Ueki S, et al. Mizuo phenomenon observed by scanning laser ophthalmoscopy in a patient with Oguchi disease. Am J Ophthalmol, 2000,130:359-361.
3Huang L,Li W,Tang W,et al.A Chinese family with Oguchi's disease due to compound heterozygosity including a novel deletion in the arrestin gene.Mol Vis,2012,18:528-536.
7Fujinami K,Tsunoda K,Nakamura M,et al.Oguchi disease with unusual findings associated with a heterozygous mutation in the SAG gene.Arch Ophthalnol,2011,129:1375-1376.
8Azam M,Collin RW,Khan MI,et al.A novel mutation in GRK1 causes Oguchi disease in a consanguineous Pakistani family.Mol Vis,2009,15:1788-1793.
9Oishi A,Akimoto M,Kawagoe N,et al.Novel mutations in the GRK1 gene in Japanese patients With Oguchi disease.Am J Ophthalmol,2007,144:475-477.
10Hayashi T,Gekka T,Takeuchi T,et al.A novel homozygous GRK1 mutation (P391H) in 2 siblings with Oguchi disease with markedly reduced cone responses.Ophthalmology,2007,114:134-141.
