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No association between the rs10503253 polymorphism in the CSMD1 gene and schizophrenia in a Han Chinese population

BACKGROUND: Schizophrenia (SCZ) is a complex, heritable, and devastating psychiatric disorder. Recent genome-wide association studies have identified a single-nucleotide polymorphism (SNP; rs10503253) in the CUB and SUSHI multiple domains 1 (CSMD1) gene as a risk factor for SCZ. In this study, we in...

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Detalles Bibliográficos
Autores principales: Liu, Yansong, Cheng, Zaohuo, Wang, Jun, Jin, Chunhui, Yuan, Jianmin, Wang, Guoqiang, Zhang, Fuquan, Zhao, Xudong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4932686/
https://www.ncbi.nlm.nih.gov/pubmed/27377754
http://dx.doi.org/10.1186/s12888-016-0923-5
Descripción
Sumario:BACKGROUND: Schizophrenia (SCZ) is a complex, heritable, and devastating psychiatric disorder. Recent genome-wide association studies have identified a single-nucleotide polymorphism (SNP; rs10503253) in the CUB and SUSHI multiple domains 1 (CSMD1) gene as a risk factor for SCZ. In this study, we investigated whether the rs10503253 in CSMD1 contributes to the risk of SCZ in a Han Chinese population. METHODS: We conducted a case-control study in a population from eastern China, involving 1378 SCZ patients and 1091 unrelated healthy controls, using the ligase detection reaction–polymerase chain reaction method to genotype the rs10503253 polymorphism in the CSMD1 gene. RESULTS: No significant association was found between the SCZ patients and controls for any allele or genotype frequency of the SNP rs10503253 (all P > 0.05). CONCLUSIONS: Our findings do not support an association between CSMD1 rs10503253 and SCZ in a Han Chinese population.