DCTN1-related neurodegeneration: Perry syndrome and beyond

Perry syndrome (PS) is a rare hereditary neurodegenerative disease characterized by autosomal dominant parkinsonism, psychiatric symptoms, weight loss, central hypoventilation, and distinct TDP-43 pathology. The mutated causative gene for PS is DCTN1, which encodes the dynactin subunit p150(Glued)....

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Bibliographic Details
Published in:Parkinsonism Relat Disord
Main Authors: Konno, Takuya, Ross, Owen A., Teive, Hélio A.G., Sławek, Jarosław, Dickson, Dennis W., Wszolek, Zbigniew K.
Format: Artigo
Language:Inglês
Published: 2017
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Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC5546300/
https://ncbi.nlm.nih.gov/pubmed/28625595
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.parkreldis.2017.06.004
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