Cargando…
Genetic Association Study of KCNQ5 Polymorphisms with High Myopia
Identification of genetic variations related to high myopia may advance our knowledge of the etiopathogenesis of refractive error. This study investigated the role of potassium channel gene (KCNQ5) polymorphisms in high myopia. We performed a case-control study of 1563 unrelated Han Chinese subjects...
Autores principales: | Liao, Xuan, Yap, Maurice K. H., Leung, Kim Hung, Kao, Patrick Y. P., Liu, Long Qian, Yip, Shea Ping |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5572591/ https://www.ncbi.nlm.nih.gov/pubmed/28884119 http://dx.doi.org/10.1155/2017/3024156 |
Ejemplares similares
-
Linkage and association of myocilin (MYOC) polymorphisms with high myopia in a Chinese population
por: Tang, Wing Chun, et al.
Publicado: (2007) -
PAX6 Haplotypes Are Associated with High Myopia in Han Chinese
por: Jiang, Bo, et al.
Publicado: (2011) -
Association of High Myopia with Crystallin Beta A4 (CRYBA4) Gene Polymorphisms in the Linkage-Identified MYP6 Locus
por: Ho, Daniel W. H., et al.
Publicado: (2012) -
Genetic Susceptibility to Refractive Error: Association of Vasoactive Intestinal Peptide Receptor 2 (VIPR2) with High Myopia in Chinese
por: Yiu, Wai Chi, et al.
Publicado: (2013) -
Investigating the relationship between UMODL1 gene polymorphisms and high myopia: a case–control study in Chinese
por: Zhu, Miao-miao, et al.
Publicado: (2012)