Assessment of the retinal posterior pole in dominant optic atrophy by spectral-domain optical coherence tomography and microperimetry

Author:

Cesareo Massimo,Ciuffoletti Elena,Martucci Alessio,Sebastiani Jacopo,Sorge Roberto Pietro,Lamantea Eleonora,Garavaglia Barbara,Ricci Federico,Cusumano Andrea,Nucci Carlo,Brancati Francesco

Funder

Fondazione Pierfranco e Luisa Mariani

Mitocon ONLUS

Cell line and DNA Bank of Genetic Movement Disorders and Mitochondrial Diseases” of Telethon Network of Genetics Biobanks

Macula and Genoma Foundation

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

Reference41 articles.

1. Dominant optic atrophy mapped to chromosome 3q region. II. Clinical and epidemiological aspects;B Kjer;Acta Ophthalmol Scand,1996

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

3. Visual prognosis in autosomal dominant optic atrophy (Kjer type);D Eliott;Am J Ophthalmol,1993

4. Clinical features in affected individuals from 21 pedigrees with dominant optic atrophy;M Votruba;Arch Ophthalmol,1998

5. Dominant optic atrophy. Refining the clinical diagnostic criteria in light of genetic linkage studies;RL Johnston;Ophthalmology,1999

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