| Literature DB >> 16644365 |
Michel Michaelides1, Alison J Hardcastle, David M Hunt, Anthony T Moore.
Abstract
The cone and cone-rod dystrophies form part of a heterogeneous group of retinal disorders that are an important cause of visual impairment in children and adults. There have been considerable advances made in recent years in our understanding of the pathogenesis of these retinal dystrophies, with many of the chromosomal loci and causative genes having now been identified. Mutations in 12 genes, including GUCA1A, peripherin/RDS, ABCA4 and RPGR, have been described to date; and in many cases detailed functional assessment of the effects of the encoded mutant proteins has been undertaken. This improved knowledge of disease mechanisms has raised the possibility of future treatments for these disorders, for which there are no specific therapies available at the present time.Entities:
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Year: 2006 PMID： 16644365 DOI： 10.1016/j.survophthal.2006.02.007
Source DB: PubMed Journal: Surv Ophthalmol ISSN： 0039-6257 Impact factor: 6.048