Dysregulation of genes coding for proteins involved in metabolic processes in mucopolysaccharidoses, evidenced by a transcriptomic approach

Mucopolysaccharidoses (MPS) are a group of lysosomal storage diseases (LSD) caused by mutations in genes coding for enzymes responsible for degradation of glycosaminoglycans (GAGs). Most types of these severe disorders are characterized by neuronopathic phenotypes. Although lysosomal accumulation of...

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Detalles Bibliográficos
Autores principales: Pierzynowska, Karolina, Deresz, Patrycja, Węgrzyn, Grzegorz, Gaffke, Lidia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2023
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349023/
https://www.ncbi.nlm.nih.gov/pubmed/37195412
http://dx.doi.org/10.1007/s11011-023-01231-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10349023/
https://www.ncbi.nlm.nih.gov/pubmed/37195412
http://dx.doi.org/10.1007/s11011-023-01231-5

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