Perry Syndrome: A Distinctive Type of TDP-43 Proteinopathy

Perry syndrome is a rare atypical parkinsonism with depression, apathy, weight loss, and central hypoventilation caused by mutations in dynactin p150(glued) (DCTN1). A rare distal hereditary motor neuropathy, HMN7B, also has mutations in DCTN1. Perry syndrome has TAR DNA-binding protein of 43 kDa (T...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:J Neuropathol Exp Neurol
Prif Awduron: Mishima, Takayasu, Koga, Shunsuke, Lin, Wen-Lang, Kasanuki, Koji, Castanedes-Casey, Monica, Wszolek, Zbigniew K., Oh, Shin J., Tsuboi, Yoshio, Dickson, Dennis W.
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Oxford University Press 2017
Pynciau:
Original Articles
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC5901076/
https://ncbi.nlm.nih.gov/pubmed/28789478
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/jnen/nlx049
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