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...

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Detalles Bibliográficos
Autores principales: Hama, Yuka, Katsu, Masataka, Takigawa, Ichigaku, Yabe, Ichiro, Matsushima, Masaaki, Takahashi, Ikuko, Katayama, Takayuki, Utsumi, Jun, Sasaki, Hidenao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5708077/
https://www.ncbi.nlm.nih.gov/pubmed/29187220
http://dx.doi.org/10.1186/s13041-017-0335-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5708077/
https://www.ncbi.nlm.nih.gov/pubmed/29187220
http://dx.doi.org/10.1186/s13041-017-0335-6

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