Significant association between rare IPO11-HTR1A variants and attention deficit hyperactivity disorder in Caucasians

OBJECTIVE: We comprehensively examined the rare variants in the IPO11-HTR1A region to explore their roles in neuropsychiatric disorders. METHOD: Five hundred seventy-three to 1,181 rare SNPs in subjects of European descent and 1,234-2,529 SNPs in subjects of African descent (0 < minor allele freq...

Descrición completa

Gardado en:
Detalles Bibliográficos
Publicado en:Am J Med Genet B Neuropsychiatr Genet
Main Authors: Zuo, Lingjun, Saba, Laura, Lin, Xiandong, Tan, Yunlong, Wang, Kesheng, Krystal, John H., Tabakoff, Boris, Luo, Xingguang
Formato: Artigo
Idioma:Inglês
Publicado: 2015
Assuntos:
Article
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4851708/
https://ncbi.nlm.nih.gov/pubmed/26079129
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.b.32329
Tags: Engadir etiqueta
Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!

Títulos similares