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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...

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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

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