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Autor:
Joanna Brokowska, Estera Rintz, Zuzanna Cyske, Karolina Pierzynowska, Lidia Gaffke, Magdalena Podlacha, Dżesika Hoinkis, Grzegorz Węgrzyn
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, Vol 21, Iss 4, p 1204 (2020)
Volume 21
Issue 4
International Journal of Molecular Sciences, Vol 21, Iss 4, p 1204 (2020)
Volume 21
Issue 4
Mucopolysaccharidoses (MPS), a group of inherited metabolic disorders caused by deficiency in enzymes involved in degradation of glycosaminoglycans (GAGs), are examples (and models) of monogenic diseases. Accumulation of undegraded GAGs in lysosomes