Defect of LSS Disrupts Lens Development in Cataractogenesis

Congenital cataract is one of the leading causes of blindness in children worldwide. About one-third of congenital cataracts are caused by genetic defects. LSS, which encodes lanosterol synthase, is a causal gene for congenital cataracts. LSS is critical in preventing abnormal protein aggregation of...

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Detalles Bibliográficos
Autores principales: Zhao, Minglei, Mei, Tingfang, Shang, Bizhi, Zou, Bin, Lian, Qing, Xu, Wenchang, Wu, Keling, Lai, Yuhua, Liu, Chujun, Wei, Lai, Zhu, Jie, Zhang, Kang, Liu, Yizhi, Zhao, Ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Cell and Developmental Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8675080/
https://www.ncbi.nlm.nih.gov/pubmed/34926465
http://dx.doi.org/10.3389/fcell.2021.788422

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8675080/
https://www.ncbi.nlm.nih.gov/pubmed/34926465
http://dx.doi.org/10.3389/fcell.2021.788422

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