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)