| 1 | CORDX5, OPN1LW, OPN1MW |
| A novel missense mutation in both OPN1LW and OPN1MW cone opsin genes causes X-linked cone dystrophy (XLCOD5). | |
| Gardner JC, Webb TR, Kanuga N, Robson AG, Holder GE, Stockman A, Ripamonti C, Ebenezer ND, Ogun O, Devery S, Wright GA, Maher ER, Cheetham ME, Moore AT, Michaelides M, Hardcastle AJ. | |
| Adv Exp Med Biol 723:595-601. doi: 10.1007/978-1-4614-0631-0_76. No abstract available. 2012 | |
| 2 | CORDX5, OPN1LW, OPN1MW |
| X-linked cone dystrophy caused by mutation of the red and green cone opsins. | |
| Gardner JC, Webb TR, Kanuga N, Robson AG, Holder GE, Stockman A, Ripamonti C, Ebenezer ND, Ogun O, Devery S, Wright GA, Maher ER, Cheetham ME, Moore AT, Michaelides M, Hardcastle AJ. | |
| Am J Hum Genet 87(1):26-39. Epub 2010 Jun 24.PMID: 20579627 2010 | |