| 1 | CSNB9, GNB3 |
| Biallelic Mutations in GNB3 Cause a Unique Form of Autosomal-Recessive Congenital Stationary Night Blindness. | |
| Vincent A, Audo I, Tavares E, Maynes JT, Tumber A, Wright T, Li S, Michiels C; GNB3 Consortium, Condroyer C, MacDonald H, Verdet R, Sahel JA, Hamel CP, Zeitz C, Héon E. | |
| Am J Hum Genet 98(5):1011-9. doi: 10.1016/j.ajhg.2016.03.021. Epub 2016 Apr 7. 2016 | |