Molecular Mechanisms in Lysosomal Storage Diseases: From Pathogenesis to Therapeutic Strategies
- PMID: 35453672
- PMCID: PMC9031509
- DOI: 10.3390/biomedicines10040922
Molecular Mechanisms in Lysosomal Storage Diseases: From Pathogenesis to Therapeutic Strategies
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 [...].
Conflict of interest statement
The authors declare no conflict of interest.
References
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