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A peep into mitochondrial disorder: multifaceted from mitochondrial DNA mutations to nuclear gene modulation
Mitochondrial genome is responsible for multiple human diseases in a maternal inherited pattern, yet phenotypes of patients in a same pedigree frequently vary largely. Genes involving in epigenetic modification, RNA processing, and other biological pathways, rather than “threshold effect” and enviro...
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| Veröffentlicht in: | Protein Cell |
|---|---|
| Hauptverfasser: | , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Higher Education Press
2015
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4656216/ https://ncbi.nlm.nih.gov/pubmed/26084519 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s13238-015-0175-z |
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