ES, P., N, F., LA, F., M, M., NH, E., H, J., . . . M, A. (2022). Novel SIX6 mutations cause recessively inherited congenital cataract, microcornea, and corneal opacification with or without coloboma and microphthalmia. Molecular vision, 28, 57.
Chicago Style (17th ed.) CitationES, Panagiotou, et al. "Novel SIX6 Mutations Cause Recessively Inherited Congenital Cataract, Microcornea, and Corneal Opacification with or Without Coloboma and Microphthalmia." Molecular Vision 28 (2022): 57.
MLA (9th ed.) CitationES, Panagiotou, et al. "Novel SIX6 Mutations Cause Recessively Inherited Congenital Cataract, Microcornea, and Corneal Opacification with or Without Coloboma and Microphthalmia." Molecular Vision, vol. 28, 2022, p. 57.
Warning: These citations may not always be 100% accurate.
