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- Behn-Krappa A., Hölker I., Sandaradura de Silva U., Doerfler W. Patterns of DNA methylation are indistinguishable in different individuals over a wide range of human DNA sequences. Genomics. 1991 Sep;11(1):1–7. doi: 10.1016/0888-7543(91)90095-v. [DOI] [PubMed] [Google Scholar]
- Bundey S., Crews S. J. A study of retinitis pigmentosa in the City of Birmingham. II Clinical and genetic heterogeneity. J Med Genet. 1984 Dec;21(6):421–428. doi: 10.1136/jmg.21.6.421. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Doi T., Molday R. S., Khorana H. G. Role of the intradiscal domain in rhodopsin assembly and function. Proc Natl Acad Sci U S A. 1990 Jul;87(13):4991–4995. doi: 10.1073/pnas.87.13.4991. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dryja T. P., McGee T. L., Reichel E., Hahn L. B., Cowley G. S., Yandell D. W., Sandberg M. A., Berson E. L. A point mutation of the rhodopsin gene in one form of retinitis pigmentosa. Nature. 1990 Jan 25;343(6256):364–366. doi: 10.1038/343364a0. [DOI] [PubMed] [Google Scholar]
- Lester D. H., Inglehearn C. F., Bashir R., Ackford H., Esakowitz L., Jay M., Bird A. C., Wright A. F., Papiha S. S., Bhattacharya S. S. Linkage to D3S47 (C17) in one large autosomal dominant retinitis pigmentosa family and exclusion in another: confirmation of genetic heterogeneity. Am J Hum Genet. 1990 Sep;47(3):536–541. [PMC free article] [PubMed] [Google Scholar]
- Lyness A. L., Ernst W., Quinlan M. P., Clover G. M., Arden G. B., Carter R. M., Bird A. C., Parker J. A. A clinical, psychophysical, and electroretinographic survey of patients with autosomal dominant retinitis pigmentosa. Br J Ophthalmol. 1985 May;69(5):326–339. doi: 10.1136/bjo.69.5.326. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McWilliam P., Farrar G. J., Kenna P., Bradley D. G., Humphries M. M., Sharp E. M., McConnell D. J., Lawler M., Sheils D., Ryan C. Autosomal dominant retinitis pigmentosa (ADRP): localization of an ADRP gene to the long arm of chromosome 3. Genomics. 1989 Oct;5(3):619–622. doi: 10.1016/0888-7543(89)90031-1. [DOI] [PubMed] [Google Scholar]
- Sparkes R. S., Mohandas T., Newman S. L., Heinzmann C., Kaufman D., Zollman S., Leveille P. J., Tobin A. J., McGinnis J. F. Assignment of the rhodopsin gene to human chromosome 3. Invest Ophthalmol Vis Sci. 1986 Jul;27(7):1170–1172. [PubMed] [Google Scholar]
- Sung C. H., Davenport C. M., Hennessey J. C., Maumenee I. H., Jacobson S. G., Heckenlively J. R., Nowakowski R., Fishman G., Gouras P., Nathans J. Rhodopsin mutations in autosomal dominant retinitis pigmentosa. Proc Natl Acad Sci U S A. 1991 Aug 1;88(15):6481–6485. doi: 10.1073/pnas.88.15.6481. [DOI] [PMC free article] [PubMed] [Google Scholar]