Molecular diagnostics for retinitis pigmentosa
- 30 October 2001
- journal article
- Published by Elsevier in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 313 (1-2) , 209-215
- https://doi.org/10.1016/s0009-8981(01)00674-x
Abstract
No abstract availableKeywords
This publication has 47 references indexed in Scilit:
- A Nonsense Mutation in a Novel Gene Is Associated With Retinitis Pigmentosa in a Family Linked to the RP1 LocusHuman Molecular Genetics, 1999
- Management of Hereditary Retinal DegenerationsSurvey of Ophthalmology, 1999
- Effect of vitamin A supplementation on rhodopsin mutants threonine-17 → methionine and proline-347 → serine in transgenic mice and in cell culturesProceedings of the National Academy of Sciences, 1998
- A Randomized Trial of Vitamin A and Vitamin E Supplementation for Retinitis PigmentosaArchives of Ophthalmology (1950), 1993
- Supplemental Vitamin A Retards Loss of ERG Amplitude in Retinitis PigmentosaArchives of Ophthalmology (1950), 1993
- Rhodopsin mutations in autosomal dominant retinitis pigmentosa.Proceedings of the National Academy of Sciences, 1991
- Treatment of Chronic Macular Edema With AcetazolamideArchives of Ophthalmology (1950), 1988
- Cataract Extraction and Intraocular Lens Implantation in Patients With Retinitis Pigmentosa or Usher's SyndromeArchives of Ophthalmology (1950), 1986
- Natural Course of Retinitis Pigmentosa Over a Three-Year IntervalPublished by Elsevier ,1985
- Prevalence of Retinitis Pigmentosa in MaineAmerican Journal of Ophthalmology, 1984