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Proximal Myopathy due to m.5835G>A Mutation in Mitochondrial MT-TY Gene
Mitochondrial (mt) tRNA (MTT) gene mutations are an important cause of mitochondrial diseases and are associated with a wide range of clinical presentations. Most mutations fall into three mitochondrial tRNAs (tRNAIle, tRNALeu (UUR), and tRNALys) and are responsible for half of the mitochondrial dis...
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| Veröffentlicht in: | Case Rep Neurol Med |
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| Hauptverfasser: | , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Hindawi
2018
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6311237/ https://ncbi.nlm.nih.gov/pubmed/30643656 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2018/8406712 |
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