RareUNC13Bvariations and risk of schizophrenia: Whole-exome sequencing in a multiplex family and follow-up resequencing and a case-control study-Reference-Cited by-同舟云学术

RareUNC13Bvariations and risk of schizophrenia: Whole-exome sequencing in a multiplex family and follow-up resequencing and a case-control study

Published:2016-03-14 Issue:6 Volume:171 Page:797-805
ISSN:1552-4841
Container-title:American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Egawa Jun¹,Hoya Satoshi¹,Watanabe Yuichiro¹,Nunokawa Ayako¹²,Shibuya Masako¹,Ikeda Masashi³,Inoue Emiko¹,Okuda Shujiro⁴,Kondo Kenji³,Saito Takeo³,Kaneko Naoshi¹²,Muratake Tatsuyuki¹⁵,Igeta Hirofumi¹,Iwata Nakao³,Someya Toshiyuki¹

Affiliation:

1. Department of Psychiatry; Niigata University Graduate School of Medical and Dental Sciences; Niigata Japan

2. Oojima Hospital; Sanjo; Niigata Japan

3. Department of Psychiatry; Fujita Health University School of Medicine; Toyoake Aichi Japan

4. Division of Bioinformatics; Niigata University Graduate School of Medical and Dental Sciences; Niigata Japan

5. Furumachi Mental Clinic; Niigata Japan

Funder

Grants-in-Aid for Scientific Research

Uehara Memorial Foundation

Kanae Foundation

Schizophrenia Clinical and Basic Research

Yamaguchi Scholarship Foundation