Atypical Leber’s Optic Neuropathy
The diagnosis of Leber’s hereditary optic neuropathy (LHON) in 6 female atypical cases seen at Harvard, Emory, and Johns Hopkins Medical Centers required molecular analysis and demonstration of the 11778 mitochondrial DNA mutation for accurate confirmation.
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| Autore principale: | |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Pediatric Neurology Briefs Publishers
1993-05-01
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| Serie: | Pediatric Neurology Briefs |
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| Accesso online: | https://www.pediatricneurologybriefs.com/articles/2979 |
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