Molecular Mechanisms in Lysosomal Storage Diseases: From Pathogenesis to Therapeutic Strategies.
Journal
Biomedicines
ISSN: 2227-9059
Titre abrégé: Biomedicines
Pays: Switzerland
ID NLM: 101691304
Informations de publication
Date de publication:
17 Apr 2022
17 Apr 2022
Historique:
received:
06
04
2022
accepted:
14
04
2022
entrez:
23
4
2022
pubmed:
24
4
2022
medline:
24
4
2022
Statut:
epublish
Résumé
Lysosomal storage diseases (LSDs) are a group of metabolic diseases caused by inborn mutations of lysosomal enzymes, which lead to lysosome substrate accumulation in various cell types [...].
Identifiants
pubmed: 35453672
pii: biomedicines10040922
doi: 10.3390/biomedicines10040922
pmc: PMC9031509
pii:
doi:
Types de publication
Editorial
Langues
eng
Subventions
Organisme : Cure Sanfilippo Foundation
ID : Targeting Heparan Sulfate Proteoglycans as a Novel Therapeutic Strategy for Sanfilippo diseas-es
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