Treatment options for Leber hereditary optic neuropathy
Leber hereditary optic neuropathy (LHON) is the most common hereditary optical neuropathy caused by primary mutations in mitochondrial DNA. LHON manifests as opticnerve atrophy and loss of central vision. In about 70% of LHON cases three major mutations in mitochondrial DNA: 11778G>A/ND4, 3460G>A/N...
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| Autors principals: | , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Vilnius University Press
2018-12-01
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| Col·lecció: | Neurologijos seminarai |
| Matèries: | |
| Accés en línia: | https://www.journals.vu.lt/neurologijos_seminarai/article/view/27817 |
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