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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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| 發表在: | J Zhejiang Univ Sci B |
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| 主要作者: | |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Zhejiang University Press
2020
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| 主題: | |
| 在線閱讀: | 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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