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Significant Association Between Rare IPO11-HTR1A Variants and Attention Deficit Hyperactivity Disorder in CaucasiansZuo, Lingjun, Saba, Laura, Lin, Xiandong, Tan, Yunlong, Wang, Kesheng, Krystal, John H., Tabakoff, Boris, Luo, Xingguang 01 October 2015 (has links)
We comprehensively examined the rare variants in the IPO11-HTR1A region to explore their roles in neuropsychiatric disorders. 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
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