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
Mutations in DZIP1 and XYLT1 are associated with nonsyndromic early onset high myopia in the Korean population.
Lee JK et al.
Ophthalmic Genetics, 0
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