Transcriptome sequencing reveals aberrant alternative splicing in Huntington's disease

Huntington’s disease (HD) is an autosomal dominant neurodegenerative disorder caused by a CAG expansion in the gene-encoding Huntingtin (HTT). Transcriptome dysregulation is a major feature of HD pathogenesis, as revealed by a large body of work on gene expression profiling of tissues from human HD...

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發表在:Hum Mol Genet
Main Authors: Lin, Lan, Park, Juw Won, Ramachandran, Shyam, Zhang, Yida, Tseng, Yu-Ting, Shen, Shihao, Waldvogel, Henry J., Curtis, Maurice A., Faull, Richard L. M., Troncoso, Juan C., Pletnikova, Olga, Ross, Christopher A., Davidson, Beverly L., Xing, Yi
格式: Artigo
語言:Inglês
出版: Oxford University Press 2016
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Articles
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC5179942/
https://ncbi.nlm.nih.gov/pubmed/27378699
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddw187
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