Autosomal dominant Stargardt-like macular dystrophy: I. Clinical characterization, longitudinal follow-up, and evidence for a common ancestry in families linked to chromosome 6q14
- 1 April 1999
- journal article
- Published by Elsevier in American Journal of Ophthalmology
- Vol. 127 (4) , 426-435
- https://doi.org/10.1016/s0002-9394(98)00331-6
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Age-related Macular DegenerationArchives of Ophthalmology (1950), 1998
- Mutation of the Stargardt Disease Gene ( ABCR ) in Age-Related Macular DegenerationScience, 1997
- Clinical Features of a Stargardt-Like Dominant Progressive Macular Dystrophy With Genetic Linkage to Chromosome 6qArchives of Ophthalmology (1950), 1994
- A Dominant Stargardt's Macular Dystrophy Locus Maps to Chromosome 13q34Archives of Ophthalmology (1950), 1994
- Phenotypic Variation Including Retinitis Pigmentosa, Pattern Dystrophy, and Fundus Flavimaculatus in a Single Family With a Deletion of Codon 153 or 154 of the Peripherin/RDS GeneArchives of Ophthalmology (1950), 1993
- Long-Term Follow-Up of Dominant Macular Dystrophy with Flecks (Stargardt)Ophthalmologica, 1992
- Autosomal-dominant Fundus FlavimaculatusOphthalmology, 1990
- Dominantly Inherited Macular Dystrophy With Flecks (Stargardt)Archives of Ophthalmology (1950), 1980
- Pattern Dystrophy of the Pigment EpitheliumAmerican Journal of Ophthalmology, 1977
- Über familiäre, progressive Degeneration in der Maculagegend des AugesAlbrecht von Graefes Archiv für Ophthalmologie, 1909