Associated Papers
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
Familial Whole Exome Sequencing Study of 30 Families With Early-Onset High Myopia.
Yang E et al.
Investigative Ophthalmology & Visual Science, 2023
Whole-Exome Sequencing in a Cohort of High Myopia Patients in Northwest China.
Liu Y et al.
Frontiers in Cell and Developmental Biology, 2021
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