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...

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Опубликовано в: :Sci Rep
Главные авторы: 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
Формат: Artigo
Язык:Inglês
Опубликовано: Nature Publishing Group UK 2017
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Article
Online-ссылка: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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