Associated Papers
18 individual genes underwent variant screening in a northwest Chinese group comprised 83 probands diagnosed with early-onset high myopia.
Liu Y et al.
Plos One, 2025
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
36180177 (PubMed )
Supplement: bjo-2022-321511supp006.pdf
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
TNFRSF21 mutations cause high myopia.
Pan H et al.
Journal of Medical Genetics, 2019
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