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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...
保存先:
| 出版年: | J Zhejiang Univ Sci B |
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| 第一著者: | |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Zhejiang University Press
2020
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| 主題: | |
| オンライン･アクセス: | 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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