Candidate Gene Analysis in X-linked Congenital Nystagmus (NYS1)

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Identifier 20040331_nanos_posters_038
Title Candidate Gene Analysis in X-linked Congenital Nystagmus (NYS1)
Creator Kerrison, John B; Zack, Donald J; Maumenee, Irene H
Subject nystagmus; gene; congenital
Description Congenital idiopathic or motor nystagmus (CMN) is a genetically heterogeneous disorder with identified genetic lociat Xq26-q27, Xp11.4-p11.3, and 6p12. While there is no clinically apparent defect in the afferent visual system in these patients, it is not known whether the underlying molecular defect is located in the visual sensory system or supranuclear ocular motor system. Identification of the causative gene may allow insight into the molecular determinants of ocular motor control.
Relation is Part of NANOS 2004: Poster Presentations
Publisher Spencer S. Eccles Health Sciences Library, University of Utah
Date 2004-03-31
Type Text
Format application/pdf
Format Creation application/pdf
Source 2004 North American Neuro-Ophthalmology Society Annual Meeting
Rights Management Copyright 2004. For further information regarding the rights to this collection, please visit:
Holding Institution North American Neuro-Ophthalmology Association. NANOS Executive Office 5841 Cedar Lake Road, Suite 204, Minneapolis, MN 55416
Collection Neuro-ophthalmology Virtual Education Library: NOVEL
Language eng
ARK ark:/87278/s62v5nk4
Setname ehsl_novel_nam
Date Created 2011-12-13
Date Modified 2021-05-06
ID 181499
Reference URL
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