1. IC3D classification of corneal dystrophies—Edition 2;Weiss;Cornea,2015
2. Silva E, Dharmaraj S, Li, YY, Pina AL, Carter RC, Loyer M, et al. A missense mutation in GUCY2D acts as a genetic modifier inRPE65-related Leber congenital amaurosis.
3. Genetic modifiers of Mendelian disease Huntington’s disease and thetrinucleotide repeat disorders;Holmans;Hum Mol Genet,2017
4. PhenoModifier a genetic modifier database for elucidating the genetic basis of human phenotypic variation;Sun;Nucl Acids Res,2020
5. Reis-Bücklers’s' dystrophy. A clinico-pathological study;Rice;Br J Ophthalmol,1968