共 50 条
- [42] Characterization of RP1L1, a highly polymorphic paralog of the retinitis pigmentosa 1 (RP1) gene MOLECULAR VISION, 2003, 9 (19-20): : 129 - 137
- [43] A novel RP1 truncating mutation that causes autosomal dominant retinitis pigmentosa (ADRP) ADVANCES IN OPHTHALMOLOGY PRACTICE AND RESEARCH, 2025, 5 (01): : 41 - 48
- [44] Essential and Synergistic Roles of RP1 and RP1L1 in Rod Photoreceptor Axoneme and Retinitis Pigmentosa JOURNAL OF NEUROSCIENCE, 2009, 29 (31): : 9748 - 9760
- [45] INDUCED PLURIPOTENT STEM CELL MODELS OF RETINITIS PIGMENTOSA CAUSED BY RP1 MUTATION CLINICAL AND EXPERIMENTAL OPHTHALMOLOGY, 2018, 46 : 127 - 127
- [46] A novel RP1 mutation demonstrated in a Turkish family with autosomal recessive retinitis pigmentosa GENE REPORTS, 2018, 11 : 1 - 5