The molecular basis of human retinal and vitreoretinal diseasesWolfgang Berger(Amgen (Switzerland)), Barbara Kloeckener‐Gruissem(University of Zurich), John Neidhardt(University of Zurich)Progress in Retinal and Eye ResearchApril 1, 201010.1016/j.preteyeres.2010.03.004Cited by 607Open AccessSaveCiteExport RISWatch citationsAbstractRelated PapersMutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosaAndreas Gal, Yun Li, Debra A. Thompson et al.|Nature Genetics|2000|665Retinitis pigmentosa. The Friedenwald Lecture.Eliot L. Berson|PubMed|1993|642Loss-of-function mutations in a calcium-channel α1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindnessBech-Hansen Nt, Naylor Mj, Maybaum Ta et al.|Nature Genetics|1998|517An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindnessTim M. Strom, Gerald Nyakatura, Eckart Apfelstedt-Sylla et al.|Nature Genetics|1998|503Mutations in MKKS cause obesity, retinal dystrophy and renal malformations associated with Bardet-Biedl syndromeNicholas Katsanis, Philip L. Beales, Michael O. Woods et al.|Nature Genetics|2000|321