RNA-binding disturbances as a continuum from spinocerebellar ataxia type 2 to Parkinson disease
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- 作者：Aurore Nkiliza
- 关键词：SCA2p ; patients having ATXN2 mutation and a parkinsonian phenotype ; SCA2c ; patients having ATXN2 mutation and a cerebellar phenotype
- 刊名：Neurobiology of Disease
- 出版年：2016
- 出版时间：December 2016
- 年：2016
- 卷：96
- 期：Complete
- 页码：312-322
- 全文大小：1127 K
文摘
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- <p id="p0005">Transcriptome of parkinsonian with ATXN2 mutation pinpoint cell proliferationp>
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- <p id="p0010">RNA binding as a common feature of cerebellar/parkinsonian phenotypesp>
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- <p id="p0015">Ataxin-2 levels suggest potential role of ATXN2 mutated alleles in Parkinson's disease.p>