載入...
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...
Na minha lista:
| 發表在: | Hum Mol Genet |
|---|---|
| Main Authors: | , , , , , , , , , , , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Oxford University Press
2016
|
| 主題: | |
| 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 |
| 標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|