Variations in retinal degenerations
- 31 March 1992
- journal article
- research article
- Published by Elsevier in Current Biology
- Vol. 2 (3) , 113-115
- https://doi.org/10.1016/0960-9822(92)90238-6
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Altered chloride ion channel kinetics associated with the ΔF508 cystic fibrosis mutationNature, 1991
- 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
- Functional heterogeneity of mutant rhodopsins responsible for autosomal dominant retinitis pigmentosa.Proceedings of the National Academy of Sciences, 1991
- Ocular Findings in Patients With Autosomal Dominant Retinitis Pigmentosa and a Rhodopsin Gene Defect (Pro-23-His)Archives of Ophthalmology (1950), 1991
- Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosisCell, 1990
- A point mutation of the rhodopsin gene in one form of retinitis pigmentosaNature, 1990
- Autosomal dominant retinitis pigmentosa (ADRP): Localization of an ADRP gene to the long arm of chromosome 3Genomics, 1989
- Identification of a photoreceptor-specific mRNA encoded by the gene responsible for retinal degeneration slow (rds)Nature, 1989
- Retinitis PigmentosaOphthalmology, 1983