1. The HNF1A mutant Ala180Val: Clinical challenges in determining causality of a rare HNF1A variant in familial diabetes. (November 2017) Authors: Sagen, J.V.; Bjørkhaug, L.; Haukanes, B.I.; Grevle, L.; Molnes, J.; Nedrebø, B.G.; Søvik, O.; Njølstad, P.R.; Johansson, S.; Molven, A. Journal: Diabetes research and clinical practice Issue: Volume 133(2017) Page Start: 142 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗