1. A novel mutation of the RP1 gene (Lys778ter) associated with autosomal dominant retinitis pigmentosa. Issue 3 (1st March 2002) Authors: Dietrich, K; Jacobi, F K; Tippmann, S; Schmid, R; Zrenner, E; Wissinger, B; Apfelstedt-Sylla, E Journal: British journal of ophthalmology Issue: Volume 86:Issue 3(2002) Page Start: 328 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Analysis of 21 Stargardt's disease families confirms a major locus on chromosome 1p with evidence for non-allelic heterogeneity in a minority of cases. Issue 8 (August 1996) Authors: Weber, B H; Sander, S; Kopp, C; Walker, D; Eckstein, A; Wissinger, B; Zrenner, E; Grimm, T Journal: British journal of ophthalmology Issue: Volume 80:Issue 8(1996) Page Start: 745 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Cone and cone–rod dystrophy segregating in the same pedigree due to the same novel CRX gene mutation. Issue 8 (24th July 2008) Authors: Kitiratschky, V B D; Nagy, D; Zabel, T; Zrenner, E; Wissinger, B; Kohl, S; Jägle, H Journal: British journal of ophthalmology Issue: Volume 92:Issue 8(2008) Page Start: 1086 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Genomic rearrangements in OPA1 are frequent in patients with autosomal dominant optic atrophy. Issue 2 (30th January 2009) Authors: Fuhrmann, N; Alavi, M V; Bitoun, P; Woernle, S; Auburger, G; Leo-Kottler, B; Yu-Wai-Man, P; Chinnery, P; Wissinger, B Journal: Journal of medical genetics Issue: Volume 46:Issue 2(2009) Page Start: 136 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Novel rhodopsin mutations and genotype-phenotype correlation in patients with autosomal dominant retinitis pigmentosa. Issue 10 (16th September 2005) Authors: Schuster, A; Weisschuh, N; Jägle, H; Besch, D; Janecke, A R; Zierler, H; Tippmann, S; Zrenner, E; Wissinger, B Journal: British journal of ophthalmology Issue: Volume 89:Issue 10(2005) Page Start: 1258 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. RDS/peripherin gene mutations are frequent causes of central retinal dystrophies. Issue 8 (August 1997) Authors: Kohl, S; Christ-Adler, M; Apfelstedt-Sylla, E; Kellner, U; Eckstein, A; Zrenner, E; Wissinger, B Journal: Journal of medical genetics Issue: Volume 34:Issue 8(1997) Page Start: 620 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗