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...

Disgrifiad llawn

Manylion Llyfryddiaeth
Prif Awdur:	Huebecker, M
Awduron Eraill:	Platt, F
Fformat:	Traethawd Ymchwil
Iaith:	English
Cyhoeddwyd:	2019
Pynciau:	Molecular biology Biochemistry

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