14-fold increased prevalence of rare glucokinase gene variant carriers in unselected Danish patients with newly diagnosed type 2 diabetes

Autor: Anette P. Gjesing, Line Engelbrechtsen, Anne Cathrine B. Thuesen, Christian T. Have, Mette Hollensted, Niels Grarup, Allan Linneberg, Jens Steen Nielsen, Lotte B. Christensen, Reimar W. Thomsen, Kristoffer E. Johansson, Matteo Cagiada, Sarah Gersing, Rasmus Hartmann-Petersen, Kresten Lindorff-Larsen, Allan Vaag, Henrik T. Sørensen, Ivan Brandslund, Henning Beck-Nielsen, Oluf Pedersen, Jørgen Rungby, Torben Hansen

Publikováno v: Gjesing, A P, Engelbrechtsen, L, Cathrine B. Thuesen, A, Have, C T, Hollensted, M, Grarup, N, Linneberg, A, Steen Nielsen, J, Christensen, L B, Thomsen, R W, Johansson, K E, Cagiada, M, Gersing, S, Hartmann-Petersen, R, Lindorff-Larsen, K, Vaag, A, Sørensen, H T, Brandslund, I, Beck-Nielsen, H, Pedersen, O, Rungby, J & Hansen, T 2022, ' 14-fold increased prevalence of rare glucokinase gene variant carriers in unselected Danish patients with newly diagnosed type 2 diabetes ', Diabetes Research and Clinical Practice, vol. 194, 110159 . https://doi.org/10.1016/j.diabres.2022.110159

AimsRare variants in the glucokinase gene (GCK) cause Maturity-Onset Diabetes of the Young (MODY2/GCK-MODY). We investigated the prevalence of GCK variants, phenotypic characteristics, micro- and macrovascular disease at baseline and follow-up, and t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c3de5567ce3708f7bec625eb2130cbf
https://pure.au.dk/portal/da/publications/14fold-increased-prevalence-of-rare-glucokinase-gene-variant-carriers-in-unselected-danish-patients-with-newly-diagnosed-type-2-diabetes(48e449f1-fb13-42d7-8dfe-ef06fc7bfc8d).html