Items where authors include "Cerman, E"
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Panagiotou, ES, Fernandez-Fuentes, N, Farraj, LA et al. (10 more authors) (2022) Novel SIX6 mutations cause recessively inherited congenital cataract, microcornea, and corneal opacification with or without coloboma and microphthalmia. Molecular Vision, 28. pp. 57-69. ISSN 1090-0535