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
Effect of clinical whole exome sequencing in aetiological investigation and reproductive risk prediction for a couple with monogenic inherited diseases.
Wang Y et al.
Frontiers in Genetics, 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
Congenital Cataract and Its Genetics: The Era of Next-Generation Sequencing
Taylan Şekeroğlu H et al.
Turkish Journal of Ophthalmology, 2021
A Common Ancestral Mutation in CRYBB3 Identified in Multiple Consanguineous Families with Congenital Cataracts.
Jiao X et al.
Plos One, 2016
Whole exome sequencing in dominant cataract identifies a new causative factor, CRYBA2, and a variety of novel alleles in known genes.
Reis LM et al.
Human Genetics, 2013
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