Associated Papers
Mutation screening of γ-crystallin gene in congenital cataract patients from North India.
Fatima AE et al.
Indian Journal of Ophthalmology, 2026
Increased hydrophobicity of CRYGD p.(Ala159ProfsTer9): Suspected cause of congenital cataracts in a large Chinese family.
Lin M et al.
Molecular Genetics & Genomic Medicine, 2020
33460241 (PubMed )
Supplement: MGG3-8-e1436-s001.doc
Novel mutations in CRYGD are associated with congenital cataracts in Chinese families.
Yang G et al.
Scientific Reports, 2016
A recurrent mutation in CRYGD is associated with autosomal dominant congenital coralliform cataract in two unrelated Chinese families.
Yang G et al.
Molecular Vision, 2011
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