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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Bibliografiska uppgifter
Huvudupphovsman: da Silva Santos, CS
Övriga upphovsmän: Platt, F
Materialtyp: Lärdomsprov
Språk:English
Publicerad: 2021
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