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Autor:
Magdalena Żabińska, Lidia Gaffke, Patrycja Bielańska, Magdalena Podlacha, Estera Rintz, Zuzanna Cyske, Grzegorz Węgrzyn, Karolina Pierzynowska
Publikováno v:
Pharmaceutics, Vol 15, Iss 2, p 704 (2023)
Mucopolysaccharidoses (MPS) are rare genetic disorders belonging to the lysosomal storage diseases. They are caused by mutations in genes encoding lysosomal enzymes responsible for degrading glycosaminoglycans (GAGs). As a result, GAGs accumulate in
Externí odkaz:
https://doaj.org/article/72b76420239a4d05b4ecaac03a97de37