De novo non-synonymous TBL1XR1 mutation alters Wnt signaling activity

Here we report de novo non-synonymous single-nucleotide variants (SNVs) by conducting whole exome sequencing of 18 trios consisting of Japanese patients with sporadic schizophrenia and their parents. Among nine SNVs, we explored the functional impact of the de novo mutation in TBL1XR1 [c.30 C > G...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Sci Rep
Päätekijät: Nishi, Akira, Numata, Shusuke, Tajima, Atsushi, Zhu, Xiaolei, Ito, Koki, Saito, Atsushi, Kato, Yusuke, Kinoshita, Makoto, Shimodera, Shinji, Ono, Shinji, Ochi, Shinichiro, Imamura, Akira, Kurotaki, Naohiro, Ueno, Shu-ichi, Iwata, Nakao, Fukui, Kiyoshi, Imoto, Issei, Kamiya, Atsushi, Ohmori, Tetsuro
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Nature Publishing Group UK 2017
Aiheet:
Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5460159/
https://ncbi.nlm.nih.gov/pubmed/28588275
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-017-02792-z
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