Mapping gene associations in human mitochondria using clinical disease phenotypes.
Nuclear genes encode most mitochondrial proteins, and their mutations cause diverse and debilitating clinical disorders. To date, 1,200 of these mitochondrial genes have been recorded, while no standardized catalog exists of the associated clinical phenotypes. Such a catalog would be useful to devel...
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| Autori principali: | , , , , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Public Library of Science (PLoS)
2009-04-01
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| Serie: | PLoS Computational Biology |
| Accesso online: | https://journals.plos.org/ploscompbiol/article/file?id=10.1371/journal.pcbi.1000374&type=printable |
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