Insight into Pathogenic Mechanism Underlying the Hereditary Cataract Caused by βB2-G149V Mutation

Congenital cataracts account for approximately 5–20% of childhood blindness worldwide and 22–30% of childhood blindness in developing countries. Genetic disorders are the primary cause of congenital cataracts. In this work, we investigated the underlying molecular mechanism of G149V point missense m...

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Detalles Bibliográficos
Autores principales: Wu, Jing, Chen, Silong, Xu, Jingjie, Xu, Wanyue, Zheng, Sifan, Tian, Qing, Luo, Chenqi, Chen, Xiangjun, Shentu, Xingchao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10216223/
https://www.ncbi.nlm.nih.gov/pubmed/37238733
http://dx.doi.org/10.3390/biom13050864

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10216223/
https://www.ncbi.nlm.nih.gov/pubmed/37238733
http://dx.doi.org/10.3390/biom13050864

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