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...

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Udgivet i: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
Format: Artigo
Sprog:Inglês
Udgivet: 2015
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Article
Online adgang: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
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