Mitochondrial Ataxias: Molecular Classification and Clinical Heterogeneity
Ataxia is increasingly being recognized as a cardinal manifestation in primary mitochondrial diseases (PMDs) in both paediatric and adult patients. It can be caused by disruption of cerebellar nuclei or fibres, its connection with the brainstem, or spinal and peripheral lesions leading to propriocep...
Tallennettuna:
| Päätekijät: | , , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
MDPI AG
2022-04-01
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| Sarja: | Neurology International |
| Aiheet: | |
| Linkit: | https://www.mdpi.com/2035-8377/14/2/28 |
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