Leukocyte Imbalances in Mucopolysaccharidoses Patients

Leukocyte Imbalances in Mucopolysaccharidoses Patients

Mucopolysaccharidoses (MPSs) are rare inherited lysosomal storage diseases (LSDs) caused by deficient activity in one of the enzymes responsible for glycosaminoglycans lysosomal degradation. MPS II is caused by pathogenic mutations in the <i>IDS</i> gene, leading to deficient activity of...

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Bibliographic Details
Main Authors: Nuno Lopes, Maria L. Maia, Cátia S. Pereira, Inês Mondragão-Rodrigues, Esmeralda Martins, Rosa Ribeiro, Ana Gaspar, Patrício Aguiar, Paula Garcia, Maria Teresa Cardoso, Esmeralda Rodrigues, Elisa Leão-Teles, Roberto Giugliani, Maria F. Coutinho, Sandra Alves, M. Fátima Macedo
Format: Article
Language:English
Published: MDPI AG 2023-06-01
Series:Biomedicines
Subjects:
lysosomal storage diseases
mucopolysaccharidoses
glycosaminoglycans
leukocytes
T cells
invariant natural killer T (iNKT) cells
Online Access:https://www.mdpi.com/2227-9059/11/6/1699

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https://www.mdpi.com/2227-9059/11/6/1699

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