Walsh & Hoyt: Wilson's Disease

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Identifier wh_ch47_p2541_1
Title Walsh & Hoyt: Wilson's Disease
Creator Parashkev Nachev, PhD, MRCP(UK); Christopher Kennard, PhD, FRCP, FMed Sci
Affiliation (PN) University College London; (CK) University of Oxford
Subject Neurodegenerative Diseases; Metabolic Diseases; Adult; Wilson's Disease
Description Wilsons disease (WD) (hepatolenticular degeneration, Westphal-Strumpell disease) is a genetic disorder of autosomal-recessive inheritance, in which a dysfunction of copper metabolism leads to excessive accumulation of copper, particularly in the liver and basal ganglia.
Date 2005
Language eng
Format application/pdf
Type Text
Source Walsh and Hoyt's Clinical Neuro-Ophthalmology, 6th Edition
Relation is Part of Walsh and Hoyt's Clinical Neuro-Ophthalmology Walsh and Hoyt's Clinical Neuro-Ophthalmology
Collection Neuro-ophthalmology Virtual Education Library: NOVEL http://NOVEL.utah.edu
Publisher Wolters Kluwer Health, Philadelphia
Holding Institution Spencer S. Eccles Health Sciences Library, University of Utah, 10 N 1900 E SLC, UT 84112-5890
Rights Management Copyright 2005. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright
ARK ark:/87278/s69w3q20
Setname ehsl_novel_whts
ID 186701
Reference URL https://collections.lib.utah.edu/ark:/87278/s69w3q20
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