Cargando…
Insight from OPN1LW Gene Haplotypes into the Cause and Prevention of Myopia
Nearsightedness (myopia) is a global health problem of staggering proportions that has driven the hunt for environmental and genetic risk factors in hopes of gaining insight into the underlying mechanism and providing new avenues of intervention. Myopia is the dominant risk factor for leading causes...
Autores principales: | Neitz, Maureen, Wagner-Schuman, Melissa, Rowlan, Jessica S., Kuchenbecker, James A., Neitz, Jay |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9222437/ https://www.ncbi.nlm.nih.gov/pubmed/35741704 http://dx.doi.org/10.3390/genes13060942 |
Ejemplares similares
-
Intermixing the OPN1LW and OPN1MW Genes Disrupts the Exonic Splicing Code Causing an Array of Vision Disorders
por: Neitz, Maureen, et al.
Publicado: (2021) -
Role of a Dual Splicing and Amino Acid Code in Myopia, Cone Dysfunction and Cone Dystrophy Associated with L/M Opsin Interchange Mutations
por: Greenwald, Scott H., et al.
Publicado: (2017) -
Unique Haplotypes in OPN1LW as a Common Cause of High Myopia With or Without Protanopia: A Potential Window Into Myopic Mechanism
por: Wang, Yingwei, et al.
Publicado: (2023) -
The association between L:M cone ratio, cone opsin genes and myopia susceptibility
por: Hagen, Lene A., et al.
Publicado: (2019) -
Novel OPN1LW/OPN1MW Exon 3 Haplotype-Associated Splicing Defect in Patients with X-Linked Cone Dysfunction
por: Stingl, Katarina, et al.
Publicado: (2022)