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Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese
Human Molecular Genetics
Oxford University Press. The Journal's web site is located at
Guo, Y; Baum, LW; Sham, PC; Wong, V; Ng, PW; Lui, CHT; Sin, NC; Tsoi, TH; Tang, CSM; Kwan, JSH; Yip, BHK; Xiao, SM; Thomas, GN; Lau, YL; Yang, W; Cherny, SS; Kwan, P2012291
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