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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...
Autores principales: | 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 |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6328241/ https://www.ncbi.nlm.nih.gov/pubmed/30629617 http://dx.doi.org/10.1371/journal.pone.0210114 |
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