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Published in 2022 at "Orphanet Journal of Rare Diseases"
DOI: 10.1186/s13023-022-02211-1
Abstract: 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…
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Keywords:
enzymes associated;
molecular environment;
environment atypical;
environment ... See more keywords