Autosomal Dominant Optic Atrophy In Singapore

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Identifier 20150222_nanos_posters_059
Title Autosomal Dominant Optic Atrophy In Singapore
Creator Sharon L. Tow; Jing-Liang Loo; P. Amati-Bonneau; D. Bonneau; V. Procaccio; P. Reynier; Dan Milea
Affiliation (SLT) (JLL) (DM) Singapore National Eye, Centre, Singapore, Singapore; (SLT) (JLL) (DM) Singapore Eye Research Institute, Singapore, Singapore; (SLT) (JLL) (DM) Duke-National University of Singapore, Singapore, Singapore; (PAB) (DB) (VP) (DM) Angers University Hospital Angers, France
Subject Genetic Disease; Optic Neuropathy
Description Autosomal dominant optic atrophy (ADOA) is a ubiquitous condition causing bilateral visual loss, most commonly related to mutations in the OPA1 gene, mapped on the chromosome 3q28-q29. Recent data suggests a minimum prevalence of 4.07/100 000 in northern England while ADOA is more rarely reported in Asia. Our study aimed to detect patients with genetically confirmed ADOA in Singapore.
Date 2015-02-22
Language eng
Format application/pdf
Type Text
Source 2015 North American Neuro-Ophthalmology Society Annual Meeting
Relation is Part of NANOS 2015: Poster Presentations
Collection Neuro-ophthalmology Virtual Education Library: NOVEL http://NOVEL.utah.edu
Publisher Spencer S. Eccles Health Sciences Library, University of Utah
Holding Institution North American Neuro-Ophthalmology Association. NANOS Executive Office 5841 Cedar Lake Road, Suite 204, Minneapolis, MN 55416
Rights Management Copyright 2013. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright
ARK ark:/87278/s6t189fw
Context URL The NANOS Annual Meeting Neuro-Ophthalmology Collection: https://novel.utah.edu/collection/NAM/toc/
Setname ehsl_novel_nam
ID 184481
Reference URL https://collections.lib.utah.edu/ark:/87278/s6t189fw
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