E Apfelstedt-Sylla

A Comprehensive Survey of Sequence Variation in the ABCA4 (ABCR) Gene in Stargardt Disease and Age-Related Macular Degeneration

Andrea Rivera, Karen L. White, Heidi Stöhr et al. · The American Journal of Human Genetics · 2000 · 341 citations · Full text

Medicine, Genetics, Molecular Genetics +10

Total colourblindness is caused by mutations in the gene encoding the α-subunit of the cone photoreceptor cGMP-gated cation channel

Susanne Kohl, Tim Marx, Ian Giddings et al. · Nature Genetics · 1998 · 339 citations

Medicine, Genetics, Molecular Genetics +13

Genetics and phenotypes of RPE65 mutations in inherited retinal degeneration.

Debra A. Thompson, P Gyürüs, L L Fleischer et al. · PubMed · 2000 · 254 citations

Medicine, Genetics, Molecular Genetics +17

Multifocal electroretinography in retinitis pigmentosa

Mathias W. Seeliger, Ulf Kretschmann, E Apfelstedt-Sylla et al. · American Journal of Ophthalmology · 1998 · 114 citations

Medicine, Ophthalmology, Vision Science +14

Multifocal electroretinography in patients with Stargardt's macular dystrophy

Ulf Kretschmann, Mathias W. Seeliger, Klaus Rüether et al. · British Journal of Ophthalmology · 1998 · 91 citations · Full text

Medicine, Ophthalmology, Vision Science +15