Identifying functional variation in schizophrenia GWAS loci by pooled sequencing
Schizophrenia demonstrates high heritability in part accounted for by common simple nucleotide variants (SNV), rare copy number variants (CNV) and, most recently, rare SNVs Although heritability explained by rare SNVs and CNVs is small compared to that explained by common SNVs, rare SNVs in function...
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| Format: | Others |
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VCU Scholars Compass
2014
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| Online Access: | http://scholarscompass.vcu.edu/etd/3515 http://scholarscompass.vcu.edu/cgi/viewcontent.cgi?article=4492&context=etd |