A medley of retinal dystrophies
- 1 March 1993
- journal article
- editorial
- Published by Springer Nature in Nature Genetics
- Vol. 3 (3) , 191-192
- https://doi.org/10.1038/ng0393-191
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- A null mutation in the human peripherin/RDS gene in a family with autosomal dominant retinitis punctata albescensNature Genetics, 1993
- Complete rescue of photoreceptor dysplasia and degeneration in transgenic retinal degeneration slow (rds) miceNeuron, 1992
- Cloning of the CDNA for a novel photoreceptor membrane protein (rom-1) identifies a disk rim protein family implicated in human retinopathiesNeuron, 1992
- Retinal genetics: a nullifying effect for rhodopsinNature 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
- The human retinal degeneration slow (RDS) gene: Chromosome assignment and structure of the mRNAGenomics, 1991
- The retinal degeneration slow (rds) gene product is a photoreceptor disc membrane-associated glycoproteinNeuron, 1991
- Identification of a photoreceptor-specific mRNA encoded by the gene responsible for retinal degeneration slow (rds)Nature, 1989
- Peripherin, a New Member of the Intermediate Filament Protein FamilyDevelopmental Neuroscience, 1983