| 1 | CRYAA, ARCC1 |
| Identification of a novel, putative cataract-causing allele in CRYAA (G98R) in an Indian family. | |
| Santhiya ST, Soker T, Klopp N, Illig T, Prakash MV, Selvaraj B, Gopinath PM, Graw J. | |
| Mol Vis 12:768-73. 2006 | |
| 2 | ARCC1, CRYAA |
| A nonsense mutation (W9X) in CRYAA causes autosomal recessive cataract in an inbred Jewish Persian family. | |
| Pras E, Frydman M, Levy-Nissenbaum E, Bakhan T, Raz J, Assia EI, Goldman B, Pras E. | |
| Invest Ophthalmol Vis Sci 41(11):3511-5. 2000 | |