X-Linked Recessive Atrophic Macular Degeneration from RPGR Mutation
- 1 August 2002
- Vol. 80 (2) , 166-171
- https://doi.org/10.1006/geno.2002.6815
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- Chapter 47 Rod-cone interdependence: implications for therapy of photoreceptor cell diseasesPublished by Elsevier ,2001
- Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCRHuman Molecular Genetics, 1998
- Cone and rod function in cone degenerationsVision Research, 1997
- A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Starqardt macular dystrophyNature Genetics, 1997
- Occult Macular DystrophyAmerican Journal of Ophthalmology, 1996
- Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophyNature Genetics, 1993
- Foveal Cone Electroretinograms in Patients With Central Visual Loss of Unexplained EtiologyArchives of Ophthalmology (1950), 1992
- An Electroretinographic and Molecular Genetic Study of X-Linked Cone DegenerationAmerican Journal of Ophthalmology, 1989
- Hereditary Macular Dystrophy without Visible Fundus AbnormalityAmerican Journal of Ophthalmology, 1989
- Molecular Genetics of Human Blue Cone MonochromacyScience, 1989