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Insights into the pathogenic character of a common NUBPL branch-site mutation associated with mitochondrial disease and complex I deficiency using a yeast model
Complex I deficiencies are the most common causes of mitochondrial disorders. They can result from mutations not only in the structural subunits but also in a growing number of known assembly factors. A branch-site mutation in the human gene encoding assembly factor NUBPL has recently been associate...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The Company of Biologists Limited
2013
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3759347/ https://ncbi.nlm.nih.gov/pubmed/23828044 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.012682 |
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