A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes: results from an exome-wide association study of albuminuria

A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes: results from an exome-wide association study of albuminuria

<strong>Aims/hypothesis</strong> Identifying rare coding variants associated with albuminuria may open new avenues for preventing chronic kidney disease and end-stage renal disease, which are highly prevalent in individuals with diabetes. Efforts to identify genetic susceptibility varian...

Πλήρης περιγραφή

Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς: Ahluwalia, T, Schulz, C, Waage, J, Skaaby, T, Sandholm, N, Van Zuydam, N, Charmet, R, Bork-Jensen, J, Almgren, P, Thuesen, B, Bedin, M, Brandslund, I, Christensen, C, Linneberg, A, Ahlqvist, E, Groop, P, Hadjadj, S, Tregouet, D, Jørgensen, M, Grarup, N, Pedersen, O, Simons, M, Groop, L, Orho-Melander, M, McCarthy, M, Melander, O, Rossing, P, Kilpeläinen, T, Hansen, T
Μορφή: Journal article
Γλώσσα:English
Έκδοση: Springer Berlin Heidelberg 2018

Παρόμοια τεκμήρια