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Frequency and significance of the novel single nucleotide missense polymorphism Val109Asp in the human gene encoding omentin in Caucasian patients with type 2 diabetes mellitus or chronic inflammatory bowel diseases.
Schäffler A, Zeitoun M, Wobser H, Buechler C, Aslanidis C, Herfarth H
Cardiovasc Diabetol 2007, 6:3
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