Lysosomal dysfunction and glycosphingolipid dysregulation in rare and common neurodegenerative diseases
<p>Historically, the rare early-onset neurodegenerative lysosomal storage disorders (LSDs) have been studied as discrete metabolic diseases in their own right. However, in recent years links with more common late-onset neurodegenerative diseases, including amyotrophic lateral sclerosis (ALS...
Tác giả chính: | Huebecker, M |
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Tác giả khác: | Platt, F |
Định dạng: | Luận văn |
Ngôn ngữ: | English |
Được phát hành: |
2019
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Những chủ đề: |
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