Macular Dystrophy and Cone-Rod Dystrophy Caused by Mutations in the RP1 Gene: Extending the RP1 Disease Spectrum

Verbakel, S.K.; Huet, R.A.C. van; Hollander, A.I. den; Geerlings, M.J.; Kersten, E.; Klevering, B.J.; ... ; Nishiguchi, K.M. (2019)

Article / Letter to editor

• RP1
• phenotypic spectrum
• macular dystrophy
• cone-rod dystrophy
• retinitis pigmentosa

• All authors: Verbakel, S.K.; Huet, R.A.C. van; Hollander, A.I. den; Geerlings, M.J.; Kersten, E.; Klevering, B.J.; Klaver, C.C.W.; Plomp, A.S.; Wesseling, N.L.; Bergen, A.A.B.; Nikopoulos, K.; Rivolta, C.; Ikeda, Y.; Sonoda, K.H.; Wada, Y.; Boon, C.J.F.; Nakazawa, T.; Hoyng, C.B.; Nishiguchi, K.M.
• Date: 2019-03-31
• Journal: Investigative Ophthalmology & Visual Science
• Volume: 60
• Issue: 4
• Pages: 1192 - 1203
• DOI: doi:10.1167/iovs.18-26084