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

MLA

Napolitano, F., et al. “Autosomal-Dominant Myopia Associated to a Novel P4HA2 Missense Variant and Defective Collagen Hydroxylation.” Clinical Genetics, vol. 93, no. 5, May 2018, pp. 982–91. EBSCOhost, https://doi.org/10.1111/cge.13217.

APA

Napolitano, 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. (2018). Autosomal-dominant myopia associated to a novel P4HA2 missense variant and defective collagen hydroxylation. Clinical Genetics, 93(5), 982–991. https://doi.org/10.1111/cge.13217

Chicago

Napolitano, F, V Di Iorio, F Testa, A Tirozzi, M G Reccia, L Lombardi, O Farina, et al. 2018. “Autosomal-Dominant Myopia Associated to a Novel P4HA2 Missense Variant and Defective Collagen Hydroxylation.” Clinical Genetics 93 (5): 982–91. doi:10.1111/cge.13217.