Associated Papers
Analysis of mouse lens morphological and proteomic abnormalities following deletion of the βB3-crystallin promoter.
Rayêe D et al.
Experimental Eye Research, 2025
Genetic architecture of congenital cataracts: correlation of pathogenic variants with morphology and clinical outcomes.
Guo D et al.
Progress in Retinal and Eye Research, 2025
Analysis of mouse lens morphological and proteomic abnormalities following depletion of βB3-crystallin.
Rayêe D et al.
Biorxiv : the Preprint Server for Biology, 2024
Novel Mutation in CRYBB3 Causing Pediatric Cataract and Microphthalmia.
Zin OA et al.
Genes, 2021
34356085 (PubMed )
Supplement: genes-12-01069-s001.zip › genes-1253197-supplementary.pdf
Two Pathogenic Gene Mutations Identified Associating with Congenital Cataract and Iris Coloboma Respectively in a Chinese Family.
Li B et al.
Journal of Ophthalmology, 2020
32148946 (PubMed )
Supplement: 7054315.f1.pdf
Distribution of gene mutations in sporadic congenital cataract in a Han Chinese population.
Li D et al.
Molecular Vision, 2016
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