| 1 | CRYBB1, ARCC2 |
| Homozygous CRYBB1 deletion mutation underlies autosomal recessive congenital cataract | |
| Cohen D, Bar-Yosef U, Levy J, Gradstein L, Belfair N, Ofir R, Joshua S, Lifshitz T, Carmi R, Birk OS. | |
| Invest Ophthalmol Vis Sci. 48(5):2208-13. 2007 | |