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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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| Publicado no: | Am J Med Genet B Neuropsychiatr Genet |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2015
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| Assuntos: | |
| Acesso em linha: | 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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