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FGENE.2013.00067
FGENE.2013.00067
http://dx.doi.org/10.3389/FGENE.2013.00067
Detection and impact of rare regulatory variants in human disease.
P356
Q38113565-D936F091-2F97-4BF0-8AC0-97F0FF168DAB
P356
FGENE.2013.00067
http://dx.doi.org/10.3389/FGENE.2013.00067