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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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| Publicado no: | J Zhejiang Univ Sci B |
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| Autor principal: | |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Zhejiang University Press
2020
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| Assuntos: | |
| Acesso em linha: | 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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