Sonia Mamouni

A novel mutation of AFG3L2 might cause dominant optic atrophy in patients with mild intellectual disability

Majida Charif, G. Lenaers, C. Goizet, 2015, Front. Genet..

Cone dystrophy or macular dystrophy associated with novel autosomal dominant GUCA1A mutations

A. Richard, C. Hamel, I. Meunier, 2017, Molecular vision.

Probability of myopia in children with high refined carbohydrates consumption in France

V. Daien, M. Villain, C. Berticat, 2020, BMC Ophthalmology.