Molecular Mechanisms in Lysosomal Storage Diseases: From Pathogenesis to Therapeutic Strategies.
Biomedicines
; 10(4)2022 Apr 17.
Article
in En
| MEDLINE
| ID: mdl-35453672
ABSTRACT
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 [...].
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Type of study:
Etiology_studies
Language:
En
Journal:
Biomedicines
Year:
2022
Type:
Article
Affiliation country:
Italy