| 1 | HK1, RP79 |
| The phenotypic variability of HK1-associated retinal dystrophy | |
| Yuan Z, Li B, Xu M, Chang EY, Li H, Yang L, Wu S, Soens ZT, Li Y, Wong LC, Lewis RA, Sui R, Chen R. | |
| Sci Rep. Aug 1;7(1):7051. doi: 10.1038/s41598-017-07629-3. 2017 | |
| 2 | HK1, RP79 |
| A missense mutation in HK1 leads to autosomal dominant retinitis pigmentosa. | |
| Wang F, Wang Y, Zhang B, Zhao L, Lyubasyuk V, Wang K, Xu M, Li Y, Wu F, Wen C, Bernstein PS, Lin D, Zhu S, Wang H, Zhang K, Chen R. | |
| Invest Ophthalmol Vis Sci. Oct 14;55(11):7159-64. doi: 10.1167/iovs.14-15520 2014 | |