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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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Bibliografske podrobnosti
Principais autores: Viviana Vargas-López, Luisa F. Prada, Carlos J. Alméciga-Díaz
Format: Artigo
Jezik:Inglês
Izdano: Nature Portfolio 2024-02-01
Serija:Scientific Reports
Online dostop:https://doi.org/10.1038/s41598-024-54626-4
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