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Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Arden G. B., Barrada A., Kelsey J. H. New clinical test of retinal function based upon the standing potential of the eye. Br J Ophthalmol. 1962 Aug;46(8):449–467. doi: 10.1136/bjo.46.8.449. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jacobson S. G., Roman A. J., Cideciyan A. V., Robey M. G., Iwata T., Inana G. X-linked retinitis pigmentosa: functional phenotype of an RP2 genotype. Invest Ophthalmol Vis Sci. 1992 Dec;33(13):3481–3492. [PubMed] [Google Scholar]
- Kajiwara K., Sandberg M. A., Berson E. L., Dryja T. P. A null mutation in the human peripherin/RDS gene in a family with autosomal dominant retinitis punctata albescens. Nat Genet. 1993 Mar;3(3):208–212. doi: 10.1038/ng0393-208. [DOI] [PubMed] [Google Scholar]
- Mafei L., Fiorentini A. Electroretinographic responses to alternating gratings before and after section of the optic nerve. Science. 1981 Feb 27;211(4485):953–955. doi: 10.1126/science.7466369. [DOI] [PubMed] [Google Scholar]
- Nichols B. E., Sheffield V. C., Vandenburgh K., Drack A. V., Kimura A. E., Stone E. M. Butterfly-shaped pigment dystrophy of the fovea caused by a point mutation in codon 167 of the RDS gene. Nat Genet. 1993 Mar;3(3):202–207. doi: 10.1038/ng0393-202. [DOI] [PubMed] [Google Scholar]
- Standard for clinical electroretinography. International Standardization Committee. Arch Ophthalmol. 1989 Jun;107(6):816–819. doi: 10.1001/archopht.1989.01070010838024. [DOI] [PubMed] [Google Scholar]
- Wells J., Wroblewski J., Keen J., Inglehearn C., Jubb C., Eckstein A., Jay M., Arden G., Bhattacharya S., Fitzke F. Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy. Nat Genet. 1993 Mar;3(3):213–218. doi: 10.1038/ng0393-213. [DOI] [PubMed] [Google Scholar]
