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 [...].
2022
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]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/893015
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