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
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."
Relation is Part of NANOS 2015: Poster Presentations
Contributor Primary Sharon L Tow
Contributor Secondary Jing-Liang Loo, P Amati-Bonneau, D Bonneau, V Procaccio, P Reynier, Dan Milea
Publisher Spencer S. Eccles Health Sciences Library, University of Utah
Date 2015-02-22
Type Text
Format application/pdf
Format Creation application/pdf
Source 2015 North American Neuro-Ophthalmology Society Annual Meeting
Rights Management Copyright 2013. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright
Collection Neuro-ophthalmology Virtual Education Library: NOVEL http://NOVEL.utah.edu
ARK ark:/87278/s6t189fw
Setname ehsl_novel_nam
Date Created 2015-03-25
Date Modified 2016-08-01
ID 184481
Reference URL https://collections.lib.utah.edu/ark:/87278/s6t189fw
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