Citations for
1EVR8, KIF11
Clinical and Molecular Characterization of Familial Exudative Vitreoretinopathy Associated With Microcephaly.
Hull S, Arno G, Ostergaard P, Pontikos N, Robson AG, Webster AR, Hogg CR, Wright GA, Henderson RHH, Martin CA, Jackson AP, Mansour S, Moore AT, Michaelides M.
Am J Ophthalmol 207:87-98. doi: 10.1016/j.ajo.2019.05.001. Epub 2019 May 8. 2019
2EVR1, EVR2, EVR4, EVR5, EVR6, EVR8, FZD4, KIF11, LRP5, NDP, TSPAN12, ZNF408
Mutations in LRP5,FZD4, TSPAN12, NDP, ZNF408, or KIF11 Genes Account for 38.7% of Chinese Patients With Familial Exudative Vitreoretinopathy.
Rao FQ, Cai XB, Cheng FF, Cheng W, Fang XL, Li N, Huang XF, Li LH, Jin ZB.
Invest Ophthalmol Vis Sci 58(5):2623-2629. doi: 10.1167/iovs.16-21324. 2017
3EVR8, KIF11
Identification of novel KIF11 mutations in patients with familial exudative vitreoretinopathy and a phenotypic analysis.
Li JK, Fei P, Li Y, Huang QJ, Zhang Q, Zhang X, Rao YQ, Li J, Zhao P.
Sci Rep 6:26564. doi: 10.1038/srep26564. 2016