Blanton SH, Heckenlively JR, Cottingham AW, Friedman J, Sadler LA, Wagner M, et al. (Mar 1992). "Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8". Genomics. 11 (4): 857–69. doi:10.1016/0888-7543(91)90008-3. PMID1783394.
Daiger SP, Sullivan LS, Bowne SJ, Kennan A, Humphries P, Birch DG, et al. (2003). "Identification of the RP1 and RP10 (IMPDH1) Genes Causing Autosomal Dominant RP". Retinal Degenerations. Advances in Experimental Medicine and Biology. Vol. 533. pp. 1–11. doi:10.1007/978-1-4615-0067-4_1. ISBN978-1-4613-4909-9. PMC2583078. PMID15180241.
Daiger SP, Shankar SP, Schindler AB, Sullivan LS, Bowne SJ, King TM, et al. (2006). "Genetic factors modifying clinical expression of autosomal dominant RP". Retinal Degenerative Diseases. Advances in Experimental Medicine and Biology. Vol. 572. pp. 3–8. doi:10.1007/0-387-32442-9_1. ISBN978-0-387-28464-4. PMC2581449. PMID17249547.
Wang DY, Chan WM, Tam PO, Baum L, Lam DS, Chong KK, et al. (January 2005). "Gene mutations in retinitis pigmentosa and their clinical implications". Clinica Chimica Acta; International Journal of Clinical Chemistry. 351 (1–2): 5–16. doi:10.1016/j.cccn.2004.08.004. PMID15563868.
Daiger SP, Sullivan LS, Bowne SJ, Kennan A, Humphries P, Birch DG, et al. (2003). "Identification of the RP1 and RP10 (IMPDH1) Genes Causing Autosomal Dominant RP". Retinal Degenerations. Advances in Experimental Medicine and Biology. Vol. 533. pp. 1–11. doi:10.1007/978-1-4615-0067-4_1. ISBN978-1-4613-4909-9. PMC2583078. PMID15180241.
Daiger SP, Shankar SP, Schindler AB, Sullivan LS, Bowne SJ, King TM, et al. (2006). "Genetic factors modifying clinical expression of autosomal dominant RP". Retinal Degenerative Diseases. Advances in Experimental Medicine and Biology. Vol. 572. pp. 3–8. doi:10.1007/0-387-32442-9_1. ISBN978-0-387-28464-4. PMC2581449. PMID17249547.
pubmed.ncbi.nlm.nih.gov
Blanton SH, Heckenlively JR, Cottingham AW, Friedman J, Sadler LA, Wagner M, et al. (Mar 1992). "Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8". Genomics. 11 (4): 857–69. doi:10.1016/0888-7543(91)90008-3. PMID1783394.
Daiger SP, Sullivan LS, Bowne SJ, Kennan A, Humphries P, Birch DG, et al. (2003). "Identification of the RP1 and RP10 (IMPDH1) Genes Causing Autosomal Dominant RP". Retinal Degenerations. Advances in Experimental Medicine and Biology. Vol. 533. pp. 1–11. doi:10.1007/978-1-4615-0067-4_1. ISBN978-1-4613-4909-9. PMC2583078. PMID15180241.
Daiger SP, Shankar SP, Schindler AB, Sullivan LS, Bowne SJ, King TM, et al. (2006). "Genetic factors modifying clinical expression of autosomal dominant RP". Retinal Degenerative Diseases. Advances in Experimental Medicine and Biology. Vol. 572. pp. 3–8. doi:10.1007/0-387-32442-9_1. ISBN978-0-387-28464-4. PMC2581449. PMID17249547.
Wang DY, Chan WM, Tam PO, Baum L, Lam DS, Chong KK, et al. (January 2005). "Gene mutations in retinitis pigmentosa and their clinical implications". Clinica Chimica Acta; International Journal of Clinical Chemistry. 351 (1–2): 5–16. doi:10.1016/j.cccn.2004.08.004. PMID15563868.