Gene Expression-Related Changes in Morphologies of Organelles and Cellular Component Organization in Mucopolysaccharidoses

Mucopolysaccharidoses (MPS) are inherited metabolic diseases characterized by accumulation of incompletely degraded glycosaminoglycans (GAGs) in lysosomes. Although primary causes of these diseases are mutations in genes coding for enzymes involved in lysosomal GAG degradation, it was demonstrated t...

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Detalles Bibliográficos
Autores principales: Gaffke, Lidia, Pierzynowska, Karolina, Rintz, Estera, Cyske, Zuzanna, Giecewicz, Izabela, Węgrzyn, Grzegorz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7967209/
https://www.ncbi.nlm.nih.gov/pubmed/33803318
http://dx.doi.org/10.3390/ijms22052766

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7967209/
https://www.ncbi.nlm.nih.gov/pubmed/33803318
http://dx.doi.org/10.3390/ijms22052766

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