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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...
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| Publicado no: | PLoS One |
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| Main Authors: | , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2019
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| Assuntos: | |
| Acesso em linha: | 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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