Molecular Mechanisms in Lysosomal Storage Diseases: From Pathogenesis to Therapeutic Strategies

Biomedicines. 2022 Apr 17;10(4):922. doi: 10.3390/biomedicines10040922.

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 [...].

Publication types

  • Editorial