Identification of RELN variation p.Thr3192Ser in a Chinese family with schizophrenia-Reference-Cited by-同舟云学术

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Identification of RELN variation p.Thr3192Ser in a Chinese family with schizophrenia

Published:2016-04-13 Issue:1 Volume:6 Page:
ISSN:2045-2322
Container-title:Scientific Reports
language:en
Short-container-title:Sci Rep

Author:

Zhou Zhifan,Hu Zhengmao,Zhang Lu,Hu Zhaoting,Liu Haihong,Liu Zhening,Du Juan,Zhao Jingping,Zhou Lin,Xia Kun,Tang Bengsha,Shen Lu

Publisher

Springer Science and Business Media LLC

Subject

Multidisciplinary

Link

http://www.nature.com/articles/srep24327.pdf

Reference55 articles.

1. Lichtenstein, P. et al. Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study. Lancet 373, 234–9 (2009).

2. Sullivan, P. F., Kendler, K. S. & Neale, M. C. Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies. Arch Gen Psychiatry 60, 1187–92 (2003).

3. Sherrington, R. et al. Cloning of a gene bearing missense mutations in early-onset familial Alzheimer’s disease. Nature 375, 754–60 (1995).

4. St Clair, D. et al. Association within a family of a balanced autosomal translocation with major mental illness. Lancet 336, 13–6 (1990).

5. Millar, J. K. et al. Disruption of two novel genes by a translocation co-segregating with schizophrenia. Hum Mol Genet 9, 1415–23 (2000).

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