Convergent molecular mechanisms underlying cognitive impairment in mucopolysaccharidosis type II
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Clinical Neurology,Biochemistry
Link
https://link.springer.com/content/pdf/10.1007/s11011-021-00872-8.pdf
Reference71 articles.
1. Beck M (2011) Mucopolysaccharidosis Type II (Hunter Syndrome): Clinical Picture and Treatment. Curr Pharm Biotechnol 12:861–866. https://doi.org/10.2174/138920111795542714
2. Bigger BW, Begley DJ, Virgintino D, Pshezhetsky AV (2018) Anatomical changes and pathophysiology of the brain in mucopolysaccharidosis disorders. Mol Genet Metab 125:322–331. https://doi.org/10.1016/j.ymgme.2018.08.003
3. Bruyère J, Roy E, Ausseil J et al (2015) Heparan sulfate saccharides modify focal adhesions: Implication in mucopolysaccharidosis neuropathophysiology. J Mol Biol 427:775–791. https://doi.org/10.1016/j.jmb.2014.09.012
4. Carlin DE, Demchak B, Pratt D et al (2017) Network propagation in the cytoscape cyberinfrastructure. PLoS Comput Biol 13:1–9. https://doi.org/10.1371/journal.pcbi.1005598
5. Chan WM, Traboulsi EI, Arthur B et al (2006) Horizontal gaze palsy with progressive scoliosis can result from compound heterozygous mutations in ROBO3. J Med Genet 43:3–6. https://doi.org/10.1136/jmg.2005.035436
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