Bilateral optic atrophy with novel MTTL 3268 A>G homoplasmy - LHON variant or not?

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Identifier 20120214_nanos_posters_101
Title Bilateral optic atrophy with novel MTTL 3268 A>G homoplasmy - LHON variant or not?
Creator Ahn, Hyosook; Lim, Hyun-Tack; Lee, Hyejin; Shin, Kwanghoon; Kim, Gu-Hwan
Subject LHON; Bilateral Optic atrophy; novel mutation
Description Leber's Hereditary Optic Neuropathy is well known as a maternally inherited eye disease with symptoms of bilateral visual loss that affect generally young male, related predominantly with mitochondrial DNA mutations such as ND1 G3460A, ND4 G11778A and ND6 T14484C. With data accumulated and bio-molecular-genetic methods developed, several novel mutations were reported.
Date 2012-02-14
Language eng
Format application/pdf
Format Creation application/pdf
Type Text
Source 2012 North American Neuro-Ophthalmology Society Annual Meeting
Relation is Part of NANOS 2012: 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 2012. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright
ARK ark:/87278/s62n87sx
Context URL The NANOS Annual Meeting Neuro-Ophthalmology Collection: https://novel.utah.edu/collection/NAM/toc/
Setname ehsl_novel_nam
ID 181917
Reference URL https://collections.lib.utah.edu/ark:/87278/s62n87sx
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