Autosomal-dominant myopia associated to a novel P4HA2 missense variant and defective collagen hydroxylation

F. Napolitano, V. Di Iorio, F. Testa, A. Tirozzi, M. G. Reccia, L. Lombardi, O. Farina, F. Simonelli, F. Gianfrancesco, G. Di Iorio, M. A.B. Melone, T. Esposito, S. Sampaolo

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Medicine & Life Sciences