The relevance of lipid accumulation in lysosomal storage diseases in immune cells function
Lysosomal storage diseases (LSDs) are rare genetic diseases in which different molecules accumulate in the lysosome due to defects in lysosomal proteins. Fabry disease, Gaucher disease and Niemann-Pick disease type C (NPC) are LSDs, sphingolipidoses in which there is the accumulation of different sp...
| Autor principal: | |
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| Formato: | doctoralThesis |
| Idioma: | eng |
| Publicado em: |
2022
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| Texto completo: | http://hdl.handle.net/10773/30452 |
| País: | Portugal |
| Oai: | oai:ria.ua.pt:10773/30452 |