A Frameshift Variant in the CHST9 Gene Identified by Family-Based Whole Genome Sequencing Is Associated with Schizophrenia in Chinese Population

Recent studies imply that rare variants contribute to the risk of schizophrenia, however, the exact variants or genes responsible for this condition are largely unknown. In this study, we conducted whole genome sequencing (WGS) of 20 Chinese families. Each family consisted of at least two affected s...

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Detalles Bibliográficos
Autores principales: Chen, Jingchun, Wu, Jain-Shing, Mize, Travis, Moreno, Marvi, Hamid, Mahtab, Servin, Francisco, Bashy, Bita, Zhao, Zhongming, Jia, Peilin, Tsuang, Ming T., Kendler, Kenneth S., Xiong, Momiao, Chen, Xiangning
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6722128/
https://www.ncbi.nlm.nih.gov/pubmed/31481703
http://dx.doi.org/10.1038/s41598-019-49052-w

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6722128/
https://www.ncbi.nlm.nih.gov/pubmed/31481703
http://dx.doi.org/10.1038/s41598-019-49052-w

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