Citations for
1HK1, 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
2HK1, 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