Sensitivity to gene dosage and gene expression affects genes with copy number variants observed among neuropsychiatric diseases

BACKGROUND: Copy number variants (CNVs) have been reported to be associated with diseases, traits, and evolution. However, it is hard to determine which gene should have priority as a target for further functional experiments if a CNV is rare or a singleton. In this study, we attempted to overcome t...

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Detalhes bibliográficos
Publicado no:BMC Med Genomics
Main Authors: Yamasaki, Maria, Makino, Takashi, Khor, Seik-Soon, Toyoda, Hiromi, Miyagawa, Taku, Liu, Xiaoxi, Kuwabara, Hitoshi, Kano, Yukiko, Shimada, Takafumi, Sugiyama, Toshiro, Nishida, Hisami, Sugaya, Nagisa, Tochigi, Mamoru, Otowa, Takeshi, Okazaki, Yuji, Kaiya, Hisanobu, Kawamura, Yoshiya, Miyashita, Akinori, Kuwano, Ryozo, Kasai, Kiyoto, Tanii, Hisashi, Sasaki, Tsukasa, Honda, Makoto, Tokunaga, Katsushi
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2020
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7104509/
https://ncbi.nlm.nih.gov/pubmed/32223758
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12920-020-0699-9
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