Genetic and clinical landscape of ARR3-associated MYP26: the most common cause of Mendelian early-onset high myopia with a unique inheritance | British Journal of Ophthalmology
Electrical responses from human retinal cone pathways associate with a common genetic polymorphism implicated in myopia | PNAS
Developing New Anti-Myopia Drugs - Review of Myopia Management
Early onset X‐linked female limited high myopia in three multigenerational families caused by novel mutations in the ARR3 gene - Mazijk - 2022 - Human Mutation - Wiley Online Library
Genetic and clinical findings of panel‐based targeted exome sequencing in a northeast Chinese cohort with retinitis pigmentosa - Sun - 2020 - Molecular Genetics & Genomic Medicine - Wiley Online Library
Analysis of genetic networks regulating refractive eye development in collaborative cross progenitor strain mice reveals new genes and pathways underlying human myopia | bioRxiv
Pharmacotherapeutic candidates for myopia: A review - ScienceDirect
Mutation proportions grouped by the genes reported to cause myopia or... | Download Scientific Diagram
CIMB | Free Full-Text | Identification of miR-671-5p and Its Related Pathways as General Mechanisms of Both Form-Deprivation and Lens-Induced Myopia in Mice
Analysis of genetic networks regulating refractive eye development in collaborative cross progenitor strain mice reveals new genes and pathways underlying human myopia | BMC Medical Genomics | Full Text
Analysis of genetic networks regulating refractive eye development in collaborative cross progenitor strain mice reveals new genes and pathways underlying human myopia | BMC Medical Genomics | Full Text
JCM | Free Full-Text | Identification of a Novel Frameshift Variant of ARR3 Related to X-Linked Female-Limited Early-Onset High Myopia and Study on the Effect of X Chromosome Inactivation on the Myopia
Frontiers | Targeted NGS Platforms for Genetic Screening and Gene Discovery in Primary Immunodeficiencies
Myopia | Nature Reviews Disease Primers
ARR3 mutation identified in myopia patients. (A) Pedigree for the... | Download Scientific Diagram
Frontiers | PDE4B Proposed as a High Myopia Susceptibility Gene in Chinese Population
Post-GWAS screening of candidate genes for refractive error in mutant zebrafish models | Scientific Reports
Occurrence of a pathogenic variant, VUS or no pathogenic variant... | Download Scientific Diagram
Genes | Free Full-Text | Genetic Diagnosis for 64 Patients with Inherited Retinal Disease
IJERPH | Free Full-Text | The Incidence and Severity of Myopia in the Population of Medical Students and Its Dependence on Various Demographic Factors and Vision Hygiene Habits
Frontiers | Association of Extracellular Signal-Regulated Kinase Genes With Myopia: A Longitudinal Study of Chinese Children
Exome Sequencing Identifies ZNF644 Mutations in High Myopia | PLOS Genetics
The Genetics of Myopia | SpringerLink
Elevated MAF with higher recruitment to β/γ-crystallin gene promoters... | Download Scientific Diagram
Scleral HIF-1α is a prominent regulatory candidate for genetic and environmental interactions in human myopia pathogenesis - eBioMedicine
Navigating the current landscape of clinical genetic testing for inherited retinal dystrophies | Genetics in Medicine
The physical, biological, and genetic basis of myopia. Panel A. The... | Download Scientific Diagram
![PDF] IMI – Myopia Genetics Report | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/b28c035b685dd23a7ce6ad1d65cb121fd7a7c102/5-Table3-1.png "PDF] IMI – Myopia Genetics Report | Semantic Scholar")
PDF] IMI – Myopia Genetics Report | Semantic Scholar
