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...

ver descrição completa

Detalhes bibliográficos
Autor principal: da Silva Santos, CS
Outros Autores: Platt, F
Formato: Tese
Idioma:English
Publicado em: 2021
Assuntos: