Phát hiện một trường hợp mang đột biến A3243 thuộc hội chứng MELAS
Mitochondrial genome A3243G mutation in the tRNALeu(UUR) encodinggene (MTTL)is the main cause of mitochondrial encephalopathy, lactic acidosis and stroke-like episodes (MELAS). This mutation exists in heteroplasmic form and severity of the disease is affected by many factors including heteroplasmy...
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| Main Authors: | , , , , , |
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| Format: | Article |
| Language: | Vietnamese |
| Published: |
Đại học Quốc gia Hà Nội
2017
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| Subjects: | |
| Online Access: | http://repository.vnu.edu.vn/handle/VNU_123/60765 |
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| Institution: | Vietnam National University, Hanoi |
| Language: | Vietnamese |