Mitochondrial DNA sequence variation and haplogroup distribution in Chinese patients with LHON and m.14484T>C.
<h4>Background</h4>Leber hereditary optic neuropathy (LHON, MIM 535000) is one of the most common mitochondrial genetic disorders caused by three primary mtDNA mutations (m.3460G>A, m.11778G>A and m. 14484T>C). The clinical expression of LHON is affected by many additional facto...
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| Auteurs principaux: | , , , , , , |
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| Format: | article |
| Langue: | EN |
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Public Library of Science (PLoS)
2010
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| Accès en ligne: | https://doaj.org/article/521cea66e7ac4325ae9b1bd53113f2a7 |
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