Translational Study of Copy Number Variations in Schizophrenia

Rare copy number variations (CNVs) are part of the genetics of schizophrenia; they are highly heterogeneous and personalized. The CNV Analysis Group of the Psychiatric Genomic Consortium (PGC) conducted a large-scale analysis and discovered that recurrent CNVs at eight genetic loci were pathogenic t...

Descripción completa

Detalles Bibliográficos
Autores principales: Cheng, Min-Chih, Chien, Wei-Hsien, Huang, Yu-Shu, Fang, Ting-Hsuan, Chen, Chia-Hsiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8745588/
https://www.ncbi.nlm.nih.gov/pubmed/35008879
http://dx.doi.org/10.3390/ijms23010457

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8745588/
https://www.ncbi.nlm.nih.gov/pubmed/35008879
http://dx.doi.org/10.3390/ijms23010457

Ejemplares similares