Mutation analysis of the entire mitochondrial genome using denaturing high performance liquid chromatography
In patients with mitochondrial disease a continuously increasing number of mitochondrial DNA (mtDNA) mutations and polymorphisms have been identified. Most pathogenic mtDNA mutations are heteroplasmic, resulting in heteroduplexes after PCR amplification of mtDNA. To detect these heteroduplexes, we u...
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| Опубликовано в:: | Nucleic Acids Res |
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| Главные авторы: | , , , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Oxford University Press
2000
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| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC110805/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/11024191/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/28.20.e89 |
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