Genomic copy number variation analysis in multiple system atrophy

Genomic variation includes single-nucleotide variants, small insertions or deletions (indels), and copy number variants (CNVs). CNVs affect gene expression by altering the genome structure and transposable elements within a region. CNVs are greater than 1 kb in size; hence, CNVs can produce more var...

Täydet tiedot

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Bibliografiset tiedot
Julkaisussa:Mol Brain
Päätekijät: Hama, Yuka, Katsu, Masataka, Takigawa, Ichigaku, Yabe, Ichiro, Matsushima, Masaaki, Takahashi, Ikuko, Katayama, Takayuki, Utsumi, Jun, Sasaki, Hidenao
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2017
Aiheet:
Research
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5708077/
https://ncbi.nlm.nih.gov/pubmed/29187220
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13041-017-0335-6
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