Genotype and phenotype association in Leber’s hereditary optic neuropathy
Leber’s hereditary optic neuropathy (LHON) is one of the most common hereditary mitochondrial optic neuropathies characterized by bilateral, painless, subacute or acute loss of central vision. The disease usually develops between the ages of 15 and 35. The majority of LHON patients are men (about 9...
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| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Vilnius University Press
2020-09-01
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| Series: | Neurologijos seminarai |
| Subjects: | |
| Online Access: | https://www.journals.vu.lt/neurologijos_seminarai/article/view/27720 |
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