Iduronate-2-sulfatase interactome: validation by yeast two-hybrid assay

Mucopolysaccharidosis type II (MPS II), also known as Hunter syndrome, is a rare X-linked recessive disease caused by a deficiency of the lysosomal enzyme iduronate-2-sulfatase (IDS), which activates intracellular accumulation of nonmetabolized glycosaminoglycans such as heparan sulfate and dermatan...

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Detalles Bibliográficos
Autores principales: Benincore-Flórez, Eliana, El-Azaz, Jorge, Solarte, Gabriela Alejandra, Rodríguez, Alexander, Reyes, Luis H., Alméciga-Díaz, Carlos Javier, Cardona-Ramírez, Carolina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8913312/
https://www.ncbi.nlm.nih.gov/pubmed/35284671
http://dx.doi.org/10.1016/j.heliyon.2022.e09031

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8913312/
https://www.ncbi.nlm.nih.gov/pubmed/35284671
http://dx.doi.org/10.1016/j.heliyon.2022.e09031

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