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Disease-Associated Genetic Variation in Human Mitochondrial Protein Import
Mitochondrial dysfunction has consequences not only for cellular energy output but also for cellular signaling pathways. Mitochondrial dysfunction, often based on inherited gene variants, plays a role in devastating human conditions such as mitochondrial neuropathies, myopathies, cardiovascular diso...
Enregistré dans:
| Publié dans: | Am J Hum Genet |
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| Auteurs principaux: | , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Elsevier
2019
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6506819/ https://ncbi.nlm.nih.gov/pubmed/31051112 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2019.03.019 |
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