Elongated axial length and myopia-related fundus changes associated with the Arg130Cys mutation in the LIM2 gene in four Chinese families with congenital cataracts

BACKGROUND: Congenital cataract (CC) is a congenital abnormality characterized by lens opacity present at birth and is associated with highly heterogeneous clinical manifestations. Lens-specific integral membrane protein (LIM2) gene expression is localized to tight junctional domains of different le...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Xun, Qin, Yanli, Abudoukeremuahong, Aierxiding, Dongye, Meimei, Zhang, Xulin, Wang, Dongni, Li, Jing, Lin, Zhuoling, Yang, Yahan, Ding, Lin, Lin, Haotian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7940952/
https://www.ncbi.nlm.nih.gov/pubmed/33708862
http://dx.doi.org/10.21037/atm-20-4275

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7940952/
https://www.ncbi.nlm.nih.gov/pubmed/33708862
http://dx.doi.org/10.21037/atm-20-4275

Ejemplares similares