Associated Papers
Identification of a novel nonsense variant in ARR3 in a family with early-onset high myopia.
Yu J et al.
Genes & Genomics, 2026
The association of ARR3 genetic polymorphisms with pathologic myopia in Northern Chinese population.
Gao W et al.
Experimental Eye Research, 2025
Clinical and Molecular Landscape of GLRA2 in X-Linked Early-Onset High Myopia.
Li X et al.
Investigative Ophthalmology & Visual Science, 2025
Advances in the study of ARR3 in myopia.
Guo YM et al.
Frontiers in Cell and Developmental Biology, 2025
Pathogenic variant in the X-linked ARR3 gene associated with variable early-onset myopia.
Ediae GU et al.
American Journal of Medical Genetics. Part A, 2024
Whole-Exome Sequencing Among School-Aged Children With High Myopia.
Yu X et al.
Jama Network Open, 2023
Targeting the non-coding genome and temozolomide signature enables CRISPR-mediated glioma oncolysis.
Tan IL et al.
Cell Reports, 2023
Genetic and clinical landscape of ARR3-associated MYP26: the most common cause of Mendelian early-onset high myopia with a unique inheritance.
Wang Y et al.
The British Journal of Ophthalmology, 2023
The causal mutation in ARR3 gene for high myopia and progressive color vision defect.
Gu L et al.
Scientific Reports, 2023
Mutational investigation of 17 causative genes in a cohort of 113 families with nonsyndromic early-onset high myopia in northwestern China.
Ye M et al.
Molecular Genetics and Genomics : Mgg, 2023
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 Severity.
Xiao X et al.
Journal of Clinical Medicine, 2023
Early onset X-linked female limited high myopia in three multigenerational families caused by novel mutations in the ARR3 gene.
van Mazijk R et al.
Human Mutation, 2022
Myopia-26, the female-limited form of early-onset high myopia, occurring in a European family.
Széll N et al.
Orphanet Journal of Rare Diseases, 2021
Identification and Functional Characterization of a Novel Nonsense Variant in ARR3 in a Southern Chinese Family With High Myopia.
Yuan D et al.
Frontiers in Genetics, 2021
Mutation screening of 17 candidate genes in a cohort of 67 probands with early-onset high myopia.
Liu F et al.
Ophthalmic & Physiological Optics : the Journal of the British College of Ophthalmic Opticians (optometrists), 2020
X-linked heterozygous mutations in ARR3 cause female-limited early onset high myopia.
Xiao X et al.
Molecular Vision, 2016