Neurocognitive testing in a murine model of mucopolysaccharidosis type IIIA

Mucopolysaccharidosis type IIIA (MPS IIIA) is an inherited metabolic disorder caused by a lysosomal enzyme deficiency resulting in heparan sulphate (HS) accumulation and manifests with a progressive neurodegenerative phenotype. A naturally occurring MPS IIIA mouse model is invaluable for preclinical...

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Detalles Bibliográficos
Autores principales: Pericleous, Kleopatra, McIntyre, Chantelle, Fuller, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10276283/
https://www.ncbi.nlm.nih.gov/pubmed/37332488
http://dx.doi.org/10.1016/j.ymgmr.2023.100985

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10276283/
https://www.ncbi.nlm.nih.gov/pubmed/37332488
http://dx.doi.org/10.1016/j.ymgmr.2023.100985

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