Napolitano, F. ., Iorio, D. . , V, Testa, F. ., Tirozzi, A. ., Reccia, M. ., Lombardi, L. ., … Sampaolo, S. . (2018). Autosomal dominant myopia associated to a novel P4HA2 missense variant and defective collagen hydroxylation. Clinical Genetics. https://doi.org/10.1111/cge.13217 (Original work published 2018)