| Identifier |
wh_ch11_476-479 |
| Title |
Walsh & Hoyt: Dominant Optic Atrophy |
| Creator |
Nancy J. Newman, MD |
| Affiliation |
Emory University, Atlanta, GA |
| Subject |
Autosomal Dominant Traits; Optic Atrophy; OPA1; Hereditary Optic Neuropathies |
| Description |
Autosomal dominant optic atrophy, type Kjer (McKusick no. 165500, gene symbol OPA1) (359), is believed to be the most common of the hereditary optic neuropathies. The estimated disease prevalence is 150,000, or as high as 110,000 in Denmark (360,361). |
| 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/s67h4t5j |
| Setname |
ehsl_novel_whts |
| ID |
187406 |
| Reference URL |
https://collections.lib.utah.edu/ark:/87278/s67h4t5j |
