Caricamento...
Pathogenesis, Emerging therapeutic targets and Treatment in Sialidosis
INTRODUCTION: Sialidosis is a neurosomatic, lysosomal storage disease (LSD) caused by mutations in the NEU1 gene, encoding the lysosomal sialidase NEU1. Deficient enzyme activity results in impaired processing/degradation of sialo-glycoproteins, and accumulation of oversialylated metabolites. Sialid...
Salvato in:
| Pubblicato in: | Expert Opin Orphan Drugs |
|---|---|
| Autori principali: | , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2015
|
| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4777310/ https://ncbi.nlm.nih.gov/pubmed/26949572 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1517/21678707.2015.1025746 |
| Tags: |
Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !
|