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A novel, pathogenic dinucleotide deletion in the mitochondrial MT-TY gene causing myasthenia-like features
Mitochondrial DNA (mtDNA)-related diseases often pose a diagnostic challenge and require rigorous clinical and laboratory investigation. Pathogenic variants in the mitochondrial tRNA gene MT-TY, which encodes the tRNA(Tyr), are a rare cause of mitochondrial disease. Here we describe a novel m.5860de...
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| Yayımlandı: | Neuromuscul Disord |
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| Asıl Yazarlar: | , , , , , , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Pergamon Press
2020
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7477489/ https://ncbi.nlm.nih.gov/pubmed/32684384 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nmd.2020.06.008 |
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