Glycosphingolipid dysregulation and lysosomal dysfunction in motor neuron disease
<p>Historically, the early-onset rare neurodegenerative lysosomal storage disorders (LSDs) have been studied as discrete metabolic diseases in their own right. However, some links with common late-onset neurodegenerative diseases, including motor neurone disease (MND), have recently emerged. R...
| المؤلف الرئيسي: | |
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| مؤلفون آخرون: | |
| التنسيق: | أطروحة |
| اللغة: | English |
| منشور في: |
2021
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| الموضوعات: |