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 [...].
Molecular Mechanisms in Lysosomal Storage Diseases: From Pathogenesis to Therapeutic Strategies / De Pasquale, Valeria; Scarcella, Melania; Pavone, Luigi Michele. - In: BIOMEDICINES. - ISSN 2227-9059. - 10:4(2022), p. 922. [10.3390/biomedicines10040922]
Molecular Mechanisms in Lysosomal Storage Diseases: From Pathogenesis to Therapeutic Strategies
De Pasquale, Valeria
;Scarcella, Melania;Pavone, Luigi Michele
2022
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 [...].File in questo prodotto:
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