| Identifier |
wh_ch47_p2541_2 |
| Title |
Walsh & Hoyt: General Characterisitics |
| 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; General Characterisitics |
| Description |
The prevalence of the genetic defect in WD, which is found in all regions of the world, is estimated to be 1 in 100, and the prevalence of WD is 3 per 100,000. If both parents are heterozygotic carriers of the gene, their children have a 25% risk of being homozygous. |
| Date |
2005 |
| Language |
eng |
| Format |
application/pdf |
| Type |
Text |
| 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/s6md27mz |
| Setname |
ehsl_novel_whts |
| ID |
186691 |
| Reference URL |
https://collections.lib.utah.edu/ark:/87278/s6md27mz |
