Increased frequency of rare missense PPP1R3B variants among Danish patients with type 2 diabetes

BACKGROUND: PPP1R3B has been suggested as a candidate gene for monogenic forms of diabetes as well as type 2 diabetes (T2D) due to its association with glycaemic trait and its biological role in glycogen synthesis. OBJECTIVES: To study if rare missense variants in PPP1R3B increase the risk of maturi...

Popoln opis

Shranjeno v:
Bibliografske podrobnosti
izdano v:PLoS One
Main Authors: Niazi, Robina Khan, Sun, Jihua, Have, Christian Theil, Hollensted, Mette, Linneberg, Allan, Pedersen, Oluf, Nielsen, Jens Steen, Rungby, Jørgen, Grarup, Niels, Hansen, Torben, Gjesing, Anette Prior
Format: Artigo
Jezik:Inglês
Izdano: Public Library of Science 2019
Teme:
Research Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC6328241/
https://ncbi.nlm.nih.gov/pubmed/30629617
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0210114
Oznake: Označite
Brez oznak, prvi označite!

Podobne knjige/članki