Neuropathology in Mouse Models of Mucopolysaccharidosis Type I, IIIA and IIIB

Mucopolysaccharide diseases (MPS) are caused by deficiency of glycosaminoglycan (GAG) degrading enzymes, leading to GAG accumulation. Neurodegenerative MPS diseases exhibit cognitive decline, behavioural problems and shortened lifespan. We have characterised neuropathological changes in mouse models...

Full description

Saved in:

Bibliographic Details
Main Authors:	Wilkinson, Fiona L., Holley, Rebecca J., Langford-Smith, Kia J., Badrinath, Soumya, Liao, Aiyin, Langford-Smith, Alex, Cooper, Jonathan D., Jones, Simon A., Wraith, J. Ed, Wynn, Rob F., Merry, Catherine L. R., Bigger, Brian W.
Format:	Artigo
Language:	Inglês
Published:	Public Library of Science 2012
Subjects:	Research Article
Online Access:	https://ncbi.nlm.nih.gov/pmc/articles/PMC3338781/ https://ncbi.nlm.nih.gov/pubmed/22558223 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0035787
Tags:	Add Tag No Tags, Be the first to tag this record!

Neuropathology in Mouse Models of Mucopolysaccharidosis Type I, IIIA and IIIB

Similar Items