Cargando…
Identification of seven novel ZNF469 mutations in keratoconus patients in a Han Chinese population
PURPOSE: To test for the potential presence of novel mutations in the zinc finger protein (ZNF469) gene in patients with sporadic keratoconus (KC) from a Han Chinese population. METHODS: Fifty-three patients with primary KC, 30 patients with high myopia (HM), and 100 unrelated population-matched hea...
Autores principales: | Yu, Xiaoning, Chen, Binbin, Zhang, Xin, Shentu, Xingchao |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Vision
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5410165/ https://www.ncbi.nlm.nih.gov/pubmed/28484309 |
Ejemplares similares
-
Novel Mutations Identified in the Chinese Han Population with Keratoconus by Next-Generation Sequencing
por: Chen, Binbin, et al.
Publicado: (2022) -
Znf469 Plays a Critical Role in Regulating Synthesis of ECM: A Zebrafish Model of Brittle Cornea Syndrome
por: Bao, Jing, et al.
Publicado: (2023) -
Three novel variants identified within ECM-related genes in Chinese Han keratoconus patients
por: Xu, Xiayan, et al.
Publicado: (2020) -
Polymorphism rs13334190 in zinc finger protein 469 (ZNF469) is not a risk factor for keratoconus in a Saudi cohort
por: Kalantan, Hatem, et al.
Publicado: (2017) -
Whole-Exome Sequencing Identifies Novel Compound Heterozygous ZNF469 Mutations in Two Siblings with Mild Brittle Cornea Syndrome
por: Rolvien, Tim, et al.
Publicado: (2020)