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SREP22887
SREP22887
http://dx.doi.org/10.1038/SREP22887
Identification of OCTN2 variants and their association with phenotypes of Crohn's disease in a Korean population.
P356
Q36674906-C88D9692-DA5B-4FCA-AFF8-03C112FE7889
P356
SREP22887
http://dx.doi.org/10.1038/SREP22887