Mucopolysaccharidoses and the blood–brain barrier

Abstract Mucopolysaccharidoses comprise a set of genetic diseases marked by an enzymatic dysfunction in the degradation of glycosaminoglycans in lysosomes. There are eight clinically distinct types of mucopolysaccharidosis, some with various subtypes, based on which lysosomal enzyme is deficient and...

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Bibliographic Details
Main Authors: Onur Sahin, Hannah P. Thompson, Grant W. Goodman, Jun Li, Akihiko Urayama
Format: Article
Language:English
Published: BMC 2022-09-01
Series:Fluids and Barriers of the CNS
Subjects:
Online Access:https://doi.org/10.1186/s12987-022-00373-5