Evidence of epigenetic landscape shifts in mucopolysaccharidosis IIIB and IVA

Abstract Lysosomal storage diseases (LSDs) are a group of monogenic diseases characterized by mutations in genes coding for proteins associated with the lysosomal function. Despite the monogenic nature, LSDs patients exhibit variable and heterogeneous clinical manifestations, prompting investigation...

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Bibliographic Details
Main Authors: Viviana Vargas-López, Luisa F. Prada, Carlos J. Alméciga-Díaz
Format: Article
Language:English
Published: Nature Portfolio 2024-02-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-024-54626-4