Ocular Findings Associated With Rhodopsin Gene Codon 17 and Codon 182 Transition Mutations in Dominant Retinitis Pigmentosa
- 1 January 1992
- journal article
- case report
- Published by American Medical Association (AMA) in Archives of Ophthalmology (1950)
- Vol. 110 (1) , 54-62
- https://doi.org/10.1001/archopht.1992.01080130056026
Abstract
Research from JAMA Ophthalmology — Ocular Findings Associated With Rhodopsin Gene Codon 17 and Codon 182 Transition Mutations in Dominant Retinitis PigmentosaKeywords
This publication has 10 references indexed in Scilit:
- Mutation spectrum of the rhodopsin gene among patients with autosomal dominant retinitis pigmentosa.Proceedings of the National Academy of Sciences, 1991
- Ocular Findings in Patients with Autosomal Dominant Retinitis Pigmentosa and Rhodopsin, Proline-347-LeucineAmerican Journal of Ophthalmology, 1991
- Ocular Findings in Patients With Autosomal Dominant Retinitis Pigmentosa and a Rhodopsin Gene Defect (Pro-23-His)Archives of Ophthalmology (1950), 1991
- Mutations within the Rhodopsin Gene in Patients with Autosomal Dominant Retinitis PigmentosaNew England Journal of Medicine, 1990
- Attachment of a 40-base-pair G + C-rich sequence (GC-clamp) to genomic DNA fragments by the polymerase chain reaction results in improved detection of single-base changes.Proceedings of the National Academy of Sciences, 1989
- A simple and efficient non-organic procedure for the isolation of genomic DNA from bloodNucleic Acids Research, 1989
- Two forms of autosomal dominant primary retinitis pigmentosaDocumenta Ophthalmologica, 1981
- Rod-Cone Interaction in the Distal Human RetinaScience, 1981
- Macular Lesions Associated With Retinitis PigmentosaArchives of Ophthalmology (1950), 1977
- Fundus Flavimaculatus: A Clinical ClassificationPublished by Springer Nature ,1977