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pro vyhledávání: '"Emilia Wieszała"'
Autor:
Magdalena Machnikowska-Sokołowska, Aleksandra Myszczuk, Emilia Wieszała, Dominika Wieja-Błach, Ewa Jamroz, Justyna Paprocka
Publikováno v:
Metabolites, Vol 13, Iss 2, p 209 (2023)
Mucopolysaccharidosis 1 (MPS 1) is a group of rare lysosomal genetic disorders resulting from the accumulation of undegraded glycosaminoglycans (GAGs) leading to multiorgan damage. Neurological symptoms vary from mild to severe. Neuroimaging—mainly
Externí odkaz:
https://doaj.org/article/c65ef6253a9e422f9e3399654a20dc08
