| Identifier |
wh_ch11_p476 |
| Title |
Walsh & Hoyt: Dominant Optic Atrophy |
| Creator |
Nancy J. Newman, MD |
| Affiliation |
Emory Eye Center |
| Subject |
Optic Nerve Diseases; Genetic Diseases, Inborn; Dominant Optic Atrophy; Dominant Optic Neuropathy |
| Description |
Autosomal dominant optic atrophy, type Kjer (McKusick no. 165500, gene symbol OPA1), is believed to be the most commonof the hereditary optic neuropathies. The estimated disease prevalence is 1:50,000, or as high as 1:10,000 in Denmark. Clinical features. Pathology. Pathphysiology. |
| 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/s64t9swm |
| Setname |
ehsl_novel_whts |
| ID |
186207 |
| Reference URL |
https://collections.lib.utah.edu/ark:/87278/s64t9swm |
