Probstel, A. K. and Schaller, A. and Lieb, J. and Hench, J. and Frank, S. and Fuhr, P. and Kappos, L. and Sinnreich, M.. (2016) Mitochondrial cytopathy with common MELAS mutation presenting as multiple system atrophy mimic. Neurol Genet, 2 (6). e121.
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Official URL: https://edoc.unibas.ch/62449/
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Abstract
Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome1 is one of the most frequently inherited mitochondrial disorders. MELAS syndrome is a systemic disease with multiple organ involvement.2 The most common mutation in MELAS is the m.3243A<G mutation in the MT-TL1 gene.2.
| Faculties and Departments: | 03 Faculty of Medicine > Departement Biomedizin > Department of Biomedicine, University Hospital Basel > Neuromuscular Research (Sinnreich) |
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| UniBasel Contributors: | Sinnreich, Michael |
| Item Type: | Article, refereed |
| Article Subtype: | Research Article |
| ISSN: | 2376-7839 (Print) 2376-7839 (Linking) |
| Note: | Publication type according to Uni Basel Research Database: Journal article |
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| Last Modified: | 25 May 2020 07:59 |
| Deposited On: | 25 May 2020 07:59 |
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