Rare compound heterozygous missense SPATA7 variations and risk of schizophrenia; whole-exome sequencing in a consanguineous family with affected siblings, follow-up sequencing and a case-control study

PURPOSE: Whole-exome sequencing (WES) of multiplex families is a promising strategy for identifying causative variations for common diseases. To identify rare recessive risk variations for schizophrenia, we performed a WES study in a consanguineous family with affected siblings. We then performed fo...

Descripción completa

Detalles Bibliográficos
Autores principales: Igeta, Hirofumi, Watanabe, Yuichiro, Morikawa, Ryo, Ikeda, Masashi, Otsuka, Ikuo, Hoya, Satoshi, Koizumi, Masataka, Egawa, Jun, Hishimoto, Akitoyo, Iwata, Nakao, Someya, Toshiyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6707433/
https://www.ncbi.nlm.nih.gov/pubmed/31695380
http://dx.doi.org/10.2147/NDT.S218773

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6707433/
https://www.ncbi.nlm.nih.gov/pubmed/31695380
http://dx.doi.org/10.2147/NDT.S218773

Ejemplares similares