Rare truncating variations and risk of schizophrenia: Whole-exome sequencing in three families with affected siblings and a three-stage follow-up study in a Japanese population. (Q50548788)
Jump to navigation
Jump to search
scientific article published on 11 December 2015
Language | Label | Description | Also known as |
---|---|---|---|
English | Rare truncating variations and risk of schizophrenia: Whole-exome sequencing in three families with affected siblings and a three-stage follow-up study in a Japanese population. |
scientific article published on 11 December 2015 |
Statements
1 reference
Rare truncating variations and risk of schizophrenia: Whole-exome sequencing in three families with affected siblings and a three-stage follow-up study in a Japanese population. (English)
1 reference
Yuichiro Watanabe
Ayako Nunokawa
Masako Shibuya
Masashi Ikeda
Akitoyo Hishimoto
Kenji Kondo
Jun Egawa
Naoshi Kaneko
Tatsuyuki Muratake
Takeo Saito
Ayu Shimasaki
Hirofumi Igeta
Emiko Inoue
Satoshi Hoya
Takuro Sugai
Ichiro Sora
Toshiyuki Someya
11 December 2015
1 reference