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Molecular environment and atypical function: What do we know about enzymes associated with Mucopolysaccharidoses?
Mucopolysaccharidoses are a group of lysosomal storage disorders caused by deficiency of enzymes involved in glycosaminoglycans degradation. Relationship between mucopolysaccharidoses and related enzymes has been clarified clearly. Based on such relationship, lots of therapies have been commercializ...
Autores principales: | Kong, Weijing, Lu, Cheng, Ding, Yingxue, Meng, Yan |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8895820/ https://www.ncbi.nlm.nih.gov/pubmed/35246201 http://dx.doi.org/10.1186/s13023-022-02211-1 |
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