![Autosomal dominant myopia associated to a novel
<i>P4HA2</i>
missense variant and defective collagen hydroxylation]()
Autosomal dominant myopia associated to a novel
<i>P4HA2</i>
missense variant and defective collagen hydroxylationNapolitano, F.; Di Iorio, V.; Testa, F.; Tirozzi, A.; Reccia, M.G.; Lombardi, L.; Farina, O.; Simonelli, F.; Gianfrancesco, F.; Di Iorio, G.; Melone, M.A.B.; Esposito, T.; Sampaolo, S. · Clinical Genetics · 2018