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...

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Bibliografiske detaljer
Hovedforfatter: da Silva Santos, CS
Andre forfattere: Platt, F
Format: Thesis
Sprog:English
Udgivet: 2021
Fag: