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MGB probe assay for rapid detection of mtDNA11778 mutation in the Chinese LHON patients by real-time PCR
Objective: Leber’s hereditary optic neuropathy (LHON) is a maternally inherited degeneration of the optic nerve caused by point mutations of mitochondrial DNA (mtDNA). Many unsolved questions regarding the penetrance and pathophysiological mechanism of LHON demand efficient and reliable mutation tes...
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| Autors principals: | , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Zhejiang University Press
2008
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2491690/ https://ncbi.nlm.nih.gov/pubmed/18763310 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1631/jzus.B0820058 |
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