Associated Papers
Potential role of βB1 crystallin in cataract formation:a systematic review.
Li M et al.
Archives of Biochemistry and Biophysics, 2025
Cataract-causing Y204X mutation of crystallin protein CRYβB1 promotes its C-terminal degradation and higher-order oligomerization.
Jing X et al.
The Journal of Biological Chemistry, 2023
Case Report: A Novel Mutation in the CRYGD Gene Causing Congenital Cataract Associated with Nystagmus in a Chinese Family.
Gao Y et al.
Frontiers in Genetics, 2022
A Novel Mutation p.S93R in CRYBB1 Associated with Dominant Congenital Cataract and Microphthalmia.
Jin A et al.
Current Eye Research, 2020
[Gene mapping and mutation detection in a family with congenital nuclear cataract].
Liu P et al.
[zhonghua Yan Ke Za Zhi] Chinese Journal of Ophthalmology, 2009
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