Cargando…
SNP Variation of RELN Gene and Schizophrenia in a Chinese Population: A Hospital-Based Case–Control Study
Aims: We aimed to explore whether RELN contributes to the vulnerability and severity of clinical symptoms of schizophrenia (SZ) in a Chinese population. Methods: The following were conducted in an adult Han Chinese population from southern China: case–control association analyses of 30 representativ...
Autores principales: | Luo, Xia, Chen, Si, Xue, Li, Chen, Jian-Huan, Shi, Yan-Wei, Zhao, Hu |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6413413/ https://www.ncbi.nlm.nih.gov/pubmed/30891068 http://dx.doi.org/10.3389/fgene.2019.00175 |
Ejemplares similares
-
Identification of RELN variation p.Thr3192Ser in a Chinese family with schizophrenia
por: Zhou, Zhifan, et al.
Publicado: (2016) -
The Genetic Variation of RELN Expression in
Schizophrenia and Bipolar Disorder
por: Ovadia, Galit, et al.
Publicado: (2011) -
Generation and analysis of novel Reln‐deleted mouse model corresponding to exonic Reln deletion in schizophrenia
por: Sawahata, Masahito, et al.
Publicado: (2020) -
Association between the g.296596G > A genetic variant of RELN gene and susceptibility to autism in a Chinese Han population
por: Fu, Xiaoyan, et al.
Publicado: (2013) -
Epigenetic RELN Dysfunction in Schizophrenia and Related Neuropsychiatric Disorders
por: Guidotti, Alessandro, et al.
Publicado: (2016)