Cargando…
Exome Sequencing Identifies ZNF644 Mutations in High Myopia
Myopia is the most common ocular disorder worldwide, and high myopia in particular is one of the leading causes of blindness. Genetic factors play a critical role in the development of myopia, especially high myopia. Recently, the exome sequencing approach has been successfully used for the disease...
Autores principales: | Shi, Yi, Li, Yingrui, Zhang, Dingding, Zhang, Hao, Li, Yuanfeng, Lu, Fang, Liu, Xiaoqi, He, Fei, Gong, Bo, Cai, Li, Li, Ruiqiang, Liao, Shihuang, Ma, Shi, Lin, He, Cheng, Jing, Zheng, Hancheng, Shan, Ying, Chen, Bin, Hu, Jianbin, Jin, Xin, Zhao, Peiquan, Chen, Yiye, Zhang, Yong, Lin, Ying, Li, Xi, Fan, Yingchuan, Yang, Huanming, Wang, Jun, Yang, Zhenglin |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3111487/ https://www.ncbi.nlm.nih.gov/pubmed/21695231 http://dx.doi.org/10.1371/journal.pgen.1002084 |
Ejemplares similares
-
New ZNF644 mutations identified in patients with high myopia
por: Xiang, Xinying, et al.
Publicado: (2014) -
An association study of the COL1A1 gene and high myopia in a Han Chinese population
por: Zhang, Dingding, et al.
Publicado: (2011) -
Study of a US cohort supports the role of ZNF644 and high-grade myopia susceptibility
por: Tran-Viet, Khanh-Nhat, et al.
Publicado: (2012) -
Evaluation of MMP2 as a candidate gene for high myopia
por: Gong, Bo, et al.
Publicado: (2013) -
A novel mutation in BBS7 gene causes Bardet–Biedl syndrome in a Chinese family
por: Yang, Zhenglin, et al.
Publicado: (2008)