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Gene co-expression network analysis for identifying modules and functionally enriched pathways in SCA2
Spinocerebellar ataxia type 2 (SCA2) is an autosomal dominant neurodegenerative disease caused by CAG repeat expansion in the ATXN2 gene. The repeat resides in an encoded region of the gene resulting in polyglutamine (polyQ) expansion which has been assumed to result in gain of function, predominant...
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| 出版年: | Hum Mol Genet |
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| 主要な著者: | , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2017
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5886232/ https://ncbi.nlm.nih.gov/pubmed/28525545 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddx191 |
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