New ZNF644 mutations identified in patients with high myopia

PURPOSE: Myopia, or near-sightedness, is one of the most common human visual impairments worldwide, and high myopia is one of the leading causes of blindness. In this study, we investigated the mutation spectrum of ZNF644, a causative gene for autosomal dominant high myopia, in a high-myopia cohort...

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Detalles Bibliográficos
Autores principales: Xiang, Xinying, Wang, Tianyun, Tong, Ping, Li, Yunping, Guo, Hui, Wan, Anran, Xia, Lu, Liu, Yanling, Li, Ying, Tian, Qi, Shen, Lu, Cai, Xinzhang, Tian, Lei, Jin, Xuemin, Xia, Kun, Hu, Zhengmao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2014
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4077594/
https://www.ncbi.nlm.nih.gov/pubmed/24991186

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