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Next generation sequence analysis for mitochondrial disorders
BACKGROUND: Mitochondrial disorders can originate from mutations in one of many nuclear genes controlling the organelle function or in the mitochondrial genome (mitochondrial DNA (mtDNA)). The large numbers of potential culprit genes, together with the little guidance offered by most clinical phenot...
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| Hlavní autoři: | , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BioMed Central
2009
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2784303/ https://ncbi.nlm.nih.gov/pubmed/19852779 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/gm100 |
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