Association of genetic variants at 22q11.2 chromosomal region with cognitive performance in Japanese patients with schizophrenia

22q11.2 heterozygous multigene deletions confer an increased risk of schizophrenia with marked impairment of cognition. We explored whether genes on 22q11.2 are associated with cognitive performance in patients with idiopathic schizophrenia. A total of 240 schizophrenia patients and 240 healthy cont...

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Detalles Bibliográficos
Autores principales: Akiyama, Kazufumi, Saito, Atsushi, Saito, Satoshi, Ozeki, Yuji, Watanabe, Takashi, Fujii, Kumiko, Shimoda, Kazutaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6543121/
https://www.ncbi.nlm.nih.gov/pubmed/31193788
http://dx.doi.org/10.1016/j.scog.2019.100134

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6543121/
https://www.ncbi.nlm.nih.gov/pubmed/31193788
http://dx.doi.org/10.1016/j.scog.2019.100134

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