| 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: Walsh and Hoyt Textbook Selections Collection: https://NOVEL.utah.edu |
| Publisher |
Wolters Kluwer Health, Philadelphia |
| Holding Institution |
Spencer S. Eccles Health Sciences Library, University of Utah |
| 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 |
