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Human Mutation|January 4, 2001
Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathiesM M Sohocki, S P Daiger, S J Bowne, et al.Human Molecular Genetics|September 15, 1999
Mutations in the RP1 gene causing autosomal dominant retinitis pigmentosaS J Bowne, S P Daiger, M M Hims, et al.American Journal of Human Genetics|December 18, 1997
Spectrum of mutations in the RPGR gene that are identified in 20% of families with X-linked retinitis pigmentosaM Buraczynska, W Wu, R Fujita, et al.Nature Genetics|December 30, 1999
Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosisM M Sohocki, S J Bowne, L S Sullivan, et al.Nature Genetics|November 4, 2000
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindnessN T Bech-Hansen, M J Naylor, T A Maybaum, et al.Pageof 19