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Mitochondrial Cytochrome c Oxidase Deficiency
As with other mitochondrial respiratory chain components, marked clinical and genetic heterogeneity is observed in patients with a cytochrome c oxidase deficiency. This constitutes a considerable diagnostic challenge and raises a number of puzzling questions. So far, pathological mutations have been...
Tallennettuna:
| Julkaisussa: | Clin Sci (Lond) |
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| Päätekijät: | , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2016
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4948581/ https://ncbi.nlm.nih.gov/pubmed/26846578 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/CS20150707 |
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