Neuropathological Staging of Spinocerebellar Ataxia Type 2 by Semiquantitative 1C2‐Positive Neuron Typing. Nuclear Translocation of Cytoplasmic 1C2 Underlies Disease Progression of Spinocerebellar Ataxia Type 2

Spinocerebellar ataxia type 2 (SCA2) is a hereditary neurodegenerative disorder caused by the expansion of the trinucleotide CAG repeats encoding elongated polyglutamine tract in ataxin‐2, the SCA2 gene product. Polyglutamine diseases comprise nine genetic entities, including seven different forms o...

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Detalhes bibliográficos
Publicado no:Brain Pathol
Main Authors: Koyano, Shigeru, Yagishita, Saburo, Kuroiwa, Yoshiyuki, Tanaka, Fumiaki, Uchihara, Toshiki
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2014
Assuntos:
Research Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC8028922/
https://ncbi.nlm.nih.gov/pubmed/24674145
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/bpa.12146
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