Associated Papers
Expanding the Phenotypic and Genotypic Landscape of Nonsyndromic High Myopia: A Cross-Sectional Study in 731 Chinese Patients.
Cai XB et al.
Investigative Ophthalmology & Visual Science, 2019
Autosomal-dominant myopia associated to a novel P4HA2 missense variant and defective collagen hydroxylation.
Napolitano F et al.
Clinical Genetics, 2018
Mutations of P4HA2 encoding prolyl 4-hydroxylase 2 are associated with nonsyndromic high myopia.
Guo H et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2015
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