1. Rhodopsin mutations in autosomal dominant retinitis pigmentosa;Al-Maghtheh, M.; Gregory, C.Y.; Inglehearn, C.; Hardcastle, A.; Bhattacharya, S.S.;Hum Mutat,1993
2. Mutations in the human retinal degeneration slow (RDS) gene can cause either retinitis pigmentosa or macular dystrophy;Wells, J.; Wroblewski, J.; Keen, J.; Inglehearn, C.; Jubb, C.; Eckstein, A.;Nature Genet,1993
3. Recessive mutations in the gene encoding the, B-subunit of rod phosphodiesterase in patients with retinitis pigmentosa;McLaughlin, M.E.; Sandberg, M.A.; Berson, E.L.; Dryja, T.P.;Nature Genet,1993
4. Localization of a retroviral element within;Bowes, C.; Li, T.; Frankel, W.N.; Danciger, M.; Coffin, J.M.; Applebury, M.L.,1993
5. Identification of a nonsense mutation in the rod photoreceptor cGMP phosphodiesterase 3-subunit gene of the rd mouse;Pittler, S.J.; Baehr, W.;Proc Natl Acad Sci USA,1991