Neuroacanthocytosis Syndromes: The Clinical Perspective
The two very rare neurodegenerative diseases historically known as the “neuroacanthocytosis syndromes” are due to mutations of either VPS13A or XK. These are phenotypically similar disorders that affect primarily the basal ganglia and hence result in involuntary abnormal movements as well as neurops...
Tallennettuna:
| Päätekijät: | , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
SAGE Publishing
2023-12-01
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| Sarja: | Contact |
| Linkit: | https://doi.org/10.1177/25152564231210339 |
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