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Publikováno v:
Pathology. 51:S24
Autor:
Kerry A. Lymn, Ainslie L.K. Roberts, Cuong D. Tran, Gordon S. Howarth, Ross N. Butler, Roger Yazbeck, Wan Chin Liaw, Janice M. Fletcher, Sharon Byers, Simon Moretta, Stamatiki Kritas
Mucopolysaccharidosis type IIIA (MPS IIIA) is a lysosomal storage disorder caused by a deficiency in sulphamidase (NS), a lysosomal enzyme required for the degradation of heparan sulphate glycosaminoglycans (gags). The MPS IIIA mouse is a naturally o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15f42cfd13de329683dd44ba48f2e9ed
https://hdl.handle.net/1959.8/132763
https://hdl.handle.net/1959.8/132763