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Secondary manifestations of mitochondrial disorders
Mitochondrial disorders (MIDs) are a heterogeneous group of genetic metabolic diseases due to mutations in the mitochondrial DNA (mtDNA) or in the nuclear DNA (nDNA) (Rahman and Rahman, 2018). Some affected genes encode proteins with various functions, or structural RNAs such as transfer RNAs (tRNAs...
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| Pubblicato in: | J Zhejiang Univ Sci B |
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| Autore principale: | |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Zhejiang University Press
2020
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7383320/ https://ncbi.nlm.nih.gov/pubmed/32633113 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1631/jzus.B2000010 |
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