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...

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Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:PLoS One
Asıl Yazarlar: 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
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Public Library of Science 2019
Konular:
Research Article
Online Erişim: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
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