Lysosomal dysfunction and glycosphingolipid dysregulation in rare and common neurodegenerative diseases

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...

書誌詳細
第一著者:	Huebecker, M
その他の著者:	Platt, F
フォーマット:	学位論文
言語:	English
出版事項:	2019
主題:	Molecular biology Biochemistry

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