Association of gene polymorphisms with type 2 diabetes and its complications in Moroccan population.

The gene encodes the mannose-binding lectin protein (MBL), which is secreted by the liver. Several variants of have been found to be associated with altered serum levels and susceptibility to various chronic diseases. Defects in MBL protein polymerization that result in functional impairments and/or low serum levels may influence genetic susceptibility to type 2 diabetes (T2D) and its complications.