Gaucher disease (GD) represents a lysosomal storage disease caused by a genetic defect of the enzyme β‐glucocerebrosidase (GBA) involved in the breakdown of complex glycosphingolipids, which are important components of cell membranes.
Prevalence of type I Gaucher disease in patients with smoldering or multiple myeloma: Results from the prospective, observational CHAGAL study
Sgherza, Nicola;Musto, Pellegrino;Amendola, Angela;Vacca, Angelo;Solimando, Antonio G.;Melaccio, Assunta;
2025-01-01
Abstract
Gaucher disease (GD) represents a lysosomal storage disease caused by a genetic defect of the enzyme β‐glucocerebrosidase (GBA) involved in the breakdown of complex glycosphingolipids, which are important components of cell membranes.File in questo prodotto:
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