Early Macular Retinal Ganglion Cell Loss in Dominant Optic Atrophy: Genotype-Phenotype Correlation

Author:

Barboni Piero,Savini Giacomo,Cascavilla Maria LuciaORCID,Caporali LeonardoORCID,Milesi Jacopo,Borrelli EnricoORCID,La Morgia Chiara,Valentino Maria Lucia,Triolo GiacintoORCID,Lembo Andrea,Carta Arturo,De Negri Annamaria,Sadun FedericoORCID,Rizzo Giovanni,Parisi Vincenzo,Pierro Luisa,Bianchi Marzoli Stefania,Zeviani Massimo,Sadun Alfredo A.,Bandello Francesco,Carelli Valerio

Publisher

Elsevier BV

Subject

Ophthalmology

Reference38 articles.

1. Infantile optic atrophy with dominant mode of inheritance: a clinical and genetic study of 19 Danish families;Kjer;Acta Ophthalmol Suppl,1959

2. Hereditary optic neuropathies;Newman,2005

3. The prevalence and natural history of dominant optic atrophy due to OPA1 mutations;Yu-Wai-Man;Ophthalmology,2010

4. Cohn AC, Toomes C, Hewitt AW, et al. The natural history of OPA1-related autosomal dominant optic atrophy. Br J Ophthalmol 92(10):1333–1336.

5. Mitochondrial optic neuropathies-disease mechanisms and therapeutic strategies;Yu-Wai-Man;Prog Retin Eye Res,2011

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