Citations for
1CCDC66
Ccdc66 null mutation causes retinal degeneration and dysfunction.
Gerding WM, Schreiber S, Schulte-Middelmann T, de Castro Marques A, Atorf J, Akkad DA, Dekomien G, Kremers J, Dermietzel R, Gal A, Rülicke T, Ibrahim S, Epplen JT, Petrasch-Parwez E.
Hum Mol Genet 20(18):3620-31. doi: 10.1093/hmg/ddr282. Epub 2011 Jun 16. 2011
2CCDC66
Progressive retinal atrophy in Schapendoes dogs: mutation of the newly identified CCDC66 gene.
Dekomien G, Vollrath C, Petrasch-Parwez E, Boevé MH, Akkad DA, Gerding WM, Epplen JT.
Neurogenetics 11(2):163-74. doi: 10.1007/s10048-009-0223-z. Epub 2009 Sep 24. 2010