Cargando…
Novel Mutations Identified in the Chinese Han Population with Keratoconus by Next-Generation Sequencing
AIM: To identify novel mutations in keratoconus (KC) susceptibility genes in the Chinese Han population. METHODS: A total of fifty-two patients with primary KC were recruited. Blood samples were collected, and genomic DNA was isolated from peripheral blood leukocytes. The entire coding region, intro...
Autores principales: | Chen, Binbin, Yu, Xiaoning, Zhang, Xin, Yang, Hao, Cui, Yilei, Shentu, Xingchao |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8853779/ https://www.ncbi.nlm.nih.gov/pubmed/35186329 http://dx.doi.org/10.1155/2022/9991910 |
Ejemplares similares
-
Identification of seven novel ZNF469 mutations in keratoconus patients in a Han Chinese population
por: Yu, Xiaoning, et al.
Publicado: (2017) -
Three novel variants identified within ECM-related genes in Chinese Han keratoconus patients
por: Xu, Xiayan, et al.
Publicado: (2020) -
The impact of GJA8 SNPs on susceptibility to age-related cataract
por: Yu, Xiaoning, et al.
Publicado: (2018) -
Targeted Next-Generation Sequencing Identified Compound Heterozygous Mutations in MYO15A as the Probable Cause of Nonsyndromic Deafness in a Chinese Han Family
por: Wang, Longhao, et al.
Publicado: (2020) -
Cytoprotective role of humanin in lens epithelial cell oxidative stress-induced injury
por: Yang, Hao, et al.
Publicado: (2020)