GM2-gangliosidosis, AB variant

Update Item Information
Identifier 20150224_nanos_posters_220
Title GM2-gangliosidosis, AB variant
Creator Michael C. Brodsky; Deborah L. Renaud
Affiliation (MCB) (DLR) Mayo Clinic Department of Neurology, Rochester, MN; (MCB) (DLR) Mayo Clinic Department of Pediatrics, Rochester, MN; (MCB) Mayo Clinic Department of Ophthalmology, Rochester, MN; (DLR) Mayo Clinic Department of Medical Genetics Rochester, MN
Subject Gangliosidosis; Cherry; Red, Spot; Activator
Description GM2-gangliosidosis, AB variant is a rare form of GM2-gangliosidosis due to a deficiency of GM2 activator protein. This autosomal recessive disorder is caused by mutations in GM2A that can only be confirmed by molecular analysis.
Date 2015-02-24
Language eng
Format application/pdf
Type Text
Source 2015 North American Neuro-Ophthalmology Society Annual Meeting
Collection Neuro-Ophthalmology Virtual Education Library: NANOS Annual Meeting Collection: https://novel.utah.edu/collection/nanos-annual-meeting-collection/
Publisher North American Neuro-Ophthalmology Society
Holding Institution Spencer S. Eccles Health Sciences Library, University of Utah
Rights Management Copyright 2015. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright
ARK ark:/87278/s6wh5ww2
Setname ehsl_novel_nam
ID 184937
Reference URL https://collections.lib.utah.edu/ark:/87278/s6wh5ww2
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