Rare FBXO18 variations and risk of schizophrenia: Whole-exome sequencing in two parent-affected offspring trios followed by resequencing and case-control studies.

Autor: Hoya, Satoshi1, Watanabe, Yuichiro1,2 yuichiro@med.niigata-u.ac.jp, Hishimoto, Akitoyo3, Nunokawa, Ayako1,4, Inoue, Emiko1, Igeta, Hirofumi1, Otsuka, Ikuo3, Shibuya, Masako1,5, Egawa, Jun1, Sora, Ichiro3, Someya, Toshiyuki1
Zdroj: Psychiatry & Clinical Neurosciences. Aug2017, Vol. 71 Issue 8, p562-568. 7p.
Databáze: Academic Search Ultimate
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