Retinal dysfunction characterizes subtypes of dominant optic atrophy-Reference-Cited by-同舟云学术

Retinal dysfunction characterizes subtypes of dominant optic atrophy

Published:2017-09-19 Issue:2 Volume:96 Page:e156-e163
ISSN:1755-375X
Container-title:Acta Ophthalmologica
language:en
Short-container-title:Acta Ophthalmol

Author:

Cascavilla Maria Lucia¹,Parisi Vincenzo²,Triolo Giacinto¹,Ziccardi Lucia²,Borrelli Enrico¹,Di Renzo Antonio²,Balducci Nicole³^ORCID,Lamperti Costanza⁴,Bianchi Marzoli Stefania⁵,Darvizeh Fatima¹,Sadun Alfredo A.⁶,Carelli Valerio⁷⁸,Bandello Francesco¹,Barboni Piero¹

Affiliation:

1. Scientific Institute San Raffaele Via Olgettina; Milan Italy

2. “G.B. Bietti” Foundation - IRCCS; Rome Italy

3. Studio Oculistico d'Azeglio; Bologna Italy

4. Unit of Molecular Neurogenetics; Foundation “C. Besta” Neurological Institute-IRCCS; Milan Italy

5. Neuro-ophthalmology Unit, Department of Ophthalmology; IRCCS Istituto Auxologico Italiano; Milano Italy

6. Department of Ophthalmology; Dohene Eye Institute, UCLA; Pasadena CA USA

7. IRCCS; Istituto delle Scienze Neurologiche di Bologna; Bologna Italy

8. Neurology Unit; Department of Biomedical and Neuromotor Sciences (DIBINEM); University of Bologna; Bologna Italy

Funder

Italian Ministry of Health

Fondazione Roma

Fondazione Telethon

Publisher

Wiley

Subject

Ophthalmology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/aos.13557/fullpdf

Reference32 articles.

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2. A splice site mutation in the murine Opa1 gene features pathology of autosomal dominant optic atrophy;Alavi;Brain,2007

3. OPA1, encoding a dynamin-related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28;Alexander;Nat Genet,2000

4. Early macular retinal ganglion cell loss in dominant optic atrophy: genotype-phenotype correlation;Barboni;Am J Ophthalmol,2014

5. Retinal nerve fiber layer thickness in dominant optic atrophy measurements by optical coherence tomography and correlation with age;Barboni;Ophthalmology,2011

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