Macular Dystrophy Associated with Mutations at Codon 172 in the Human Retinal Degeneration Slow Gene
- 1 January 1994
- journal article
- Published by Elsevier in Ophthalmology
- Vol. 101 (1) , 12-22
- https://doi.org/10.1016/s0161-6420(94)31377-7
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophyNature Genetics, 1993
- Abnormal dark adaptation kinetics in autosomal dominant sector retinitis pigmentosa due to rod opsin mutation.British Journal of Ophthalmology, 1992
- A completed screen for mutations of the rhodopsin gene in a panel of patients with autosomal dominant retinitis piamentosaHuman Molecular Genetics, 1992
- A three-base-pair deletion in the peripherin–RDS gene in one form of retinitis pigmentosaNature, 1991
- Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosaNature, 1991
- Autosomal dominant retinitis pigmentosa: Four new mutations in rhodopsin, one of them in the retinal attachment siteGenomics, 1991
- Rhodopsin mutations in autosomal dominant retinitis pigmentosa.Proceedings of the National Academy of Sciences, 1991
- Rapid detection of single base mismatches as heteroduplexes on Hydrolink gelsTrends in Genetics, 1991
- Mutations within the Rhodopsin Gene in Patients with Autosomal Dominant Retinitis PigmentosaNew England Journal of Medicine, 1990
- Automated Light- and Dark- Adapted Perimetry for Evaluating Retinitis PigmentosaOphthalmology, 1986