Article
Sanfilippo Syndrome: Molecular Basis, Disease Models and Therapeutic Approaches.
International journal of molecular sciences - 22 Oct 2020
Benetó Noelia, Vilageliu Lluïsa, Grinberg Daniel, Canals Isaac
Abstract excerpt
Sanfilippo syndrome or mucopolysaccharidosis III is a lysosomal storage disorder caused by mutations in genes responsible for the degradation of heparan sulfate, a glycosaminoglycan located in the extracellular membrane. Undegraded heparan sulfate molecules accumulate within lysosomes leading to cellular dysfunction and pathology in several organs, with severe central nervous system degeneration as the main...
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