Retinitis pigmentosa associated with rhodopsin mutations: Correlation between phenotypic variability and molecular effects

Author:

Iannaccone Alessandro,Man David,Waseem Naushin,Jennings Barbara J.,Ganapathiraju Madhavi,Gallaher Kevin,Reese Elisheva,Bhattacharya Shomi S.,Klein-Seetharaman Judith

Publisher

Elsevier BV

Subject

Sensory Systems,Ophthalmology

Reference50 articles.

1. Apáthy, P. P., Jacobson, S. G., Nghiem-Phu, L., Knighton, R. W., & Parel, J.-M. (1987). Computer-aided analysis in automated dark-adapted static perimetry. In Seventh international visual field symposium (pp. 278–284). Amsterdam, September 1986: Martinus Nijhoff/Dr. W. Junk Publishers, Dordrecht.

2. Disease sequence from mutant rhodopsin allele to rod and cone photoreceptor degeneration in man;Cideciyan;Proceedings of the National Academy of Sciences USA,1998

3. In vivo dynamics of retinal injury and repair in the rhodopsin mutant dog model of human retinitis pigmentosa;Cideciyan;Proceedings of the National Academy of Sciences USA,2005

4. Structure and function in rhodopsin: replacement by alanine of cysteine residues 110 and 187, components of a conserved disulfide bond in rhodopsin, affects the light-activated metarhodopsin II state;Davidson;Proceedings of the National Academy of Sciences USA,1994

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