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

Author(s):
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.
Published
2019
Publication type
Article / Letter to editor
RP1phenotypic spectrummacular dystrophycone-rod dystrophyretinitis pigmentosa
Date issued
2019-03-31
Language
English
Is part of
Investigative Ophthalmology & Visual Science (2019), Vol. 60, no. 4, p. 1192-1203
hdl
1887/121073
doi
10.1167/iovs.18-26084