| 1 | MFRP, MPRF, NNO2 |
| Compound heterozygosity for a novel and a recurrent MFRP gene mutation in a family with the nanophthalmos-retinitis pigmentosa complex. | |
| Zenteno JC, Buentello-Volante B, Quiroz-González MA, Quiroz-Reyes MA. | |
| Mol Vis 15:1794-8.PMID: 19753314 2009 | |
| 2 | NNO2, MFRP, NLRX1, TMEM25 |
| Extreme hyperopia is the result of null mutations in MFRP, which encodes a Frizzled-related protein. | |
| Sundin OH, Leppert GS, Silva ED, Yang JM, Dharmaraj S, Maumenee IH, Santos LC, Parsa CF, Traboulsi EI, Broman KW, Dibernardo C, Sunness JS, Toy J, Weinberg EM. | |
| Proc Natl Acad Sci U S A 102(27):9553-9558. Epub 2005 Jun 23. 2005 | |