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Publikováno v:
Molecular genetics and metabolism. 92(1-2)
Mucopolysaccharidosis type IIIA (MPS IIIA) is a specific lysosomal storage disorder caused by an enzyme deficiency in sulphamidase, which is required for the degradation of heparan sulphate glycosaminoglycan (gag). This deficiency results in widespre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::402525e2b1dfcb5db7849ec2da0efccc
https://pubmed.ncbi.nlm.nih.gov/17681480
https://pubmed.ncbi.nlm.nih.gov/17681480
