Differences in MPS I and MPS II Disease Manifestations

Mucopolysaccharidosis (MPS) type I and II are two closely related lysosomal storage diseases associated with disrupted glycosaminoglycan catabolism. In MPS II, the first step of degradation of heparan sulfate (HS) and dermatan sulfate (DS) is blocked by a deficiency in the lysosomal enzyme iduronate...

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Detalles Bibliográficos
Autores principales: Hampe, Christiane S., Yund, Brianna D., Orchard, Paul J., Lund, Troy C., Wesley, Jacob, McIvor, R. Scott
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8345985/
https://www.ncbi.nlm.nih.gov/pubmed/34360653
http://dx.doi.org/10.3390/ijms22157888

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8345985/
https://www.ncbi.nlm.nih.gov/pubmed/34360653
http://dx.doi.org/10.3390/ijms22157888

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