Open AccessFrequency 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
Author(s) -
Andréas Schäffler,
Martina Zeitoun,
Hella Wobser,
Christa Buechler,
Charalampos Aslanidis,
Hans Herfarth
Publication year - 2007
Publication title -
carolina digital repository (university of north carolina at chapel hill)
Language(s) - English
DOI - 10.17615/9pb9-0s78
Subject(s) - missense mutation , single nucleotide polymorphism , type 2 diabetes mellitus , gene , polymorphism (computer science) , medicine , genetics , diabetes mellitus , biology , endocrinology , genotype , mutation