A Novel OPA1 Mutation in Autosomal Dominant Optic Atrophy

Update item information
Identifier 20150222_nanos_posters_031
Title A Novel OPA1 Mutation in Autosomal Dominant Optic Atrophy
Creator Jordan A. Margo, Jana A. Bregman, Vivian Rismondo
Subject Genetic Disease; Optic Neuropathy
Description "Autosomal dominant optic atrophy (ADOA), or Kjer's disease, often overlaps clinically with other forms of optic atrophy making diagnosis challenging. Considering the potential for ADOA to cause significant visual impairment and its high degree of penetrance, it is important to make the correct diagnosis for both the individual patient and the family members."
Relation is Part of NANOS 2015: Poster Presentations
Contributor Primary Jordan A. Margo
Contributor Secondary Jana A. Bregman, Vivian Rismondo
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/s6mh0w92
Setname ehsl_novel_nam
Date Created 2015-03-25
Date Modified 2016-08-01
ID 184467
Reference URL https://collections.lib.utah.edu/ark:/87278/s6mh0w92
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