Associated Papers
Identification of Genetic Variants Causing Paediatric Cataract in Myanmar.
Jones JL et al.
Clinical Genetics, 2025
Novel CRYGC Mutation in Conserved Ultraviolet-Protective Tryptophan (p.Trp131Arg) Is Linked to Autosomal Dominant Congenital Cataract.
Delas F et al.
International Journal of Molecular Sciences, 2023
A Novel Mutation in CRYGC Mutation Associated with Autosomal Dominant Congenital Cataracts and Microcornea.
Zhou Z et al.
Ophthalmology Science, 2022
A novel CRYGC E128* mutation underlying an autosomal dominant nuclear cataract in a south Indian kindred.
Kandaswamy DK et al.
Ophthalmic Genetics, 2020
Distribution of gene mutations in sporadic congenital cataract in a Han Chinese population.
Li D et al.
Molecular Vision, 2016
A novel nonsense mutation in CRYGC is associated with autosomal dominant congenital nuclear cataracts and microcornea.
Zhang L et al.
Molecular Vision, 2009
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