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
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-2022-321511supp010.pdf
Select a paper to view details