Type 2 diabetes variants disrupt function of SLC16A11 through two distinct mechanisms

Type 2 Diabetes (T2D) affects Latinos at twice the rate seen in populations of European descent. We recently identified a risk haplotype spanning SLC16A11 that explains ~20% of the increased T2D prevalence in Mexico. Here, through genetic fine-mapping, we define a set of tightly-linked variants like...

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Xehetasun bibliografikoak
Argitaratua izan da:Cell
Egile Nagusiak: Rusu, Victor, Hoch, Eitan, Mercader, Josep M., Tenen, Danielle E., Gymrek, Melissa, Hartigan, Christina R., DeRan, Michael, von Grotthuss, Marcin, Fontanillas, Pierre, Spooner, Alexandra, Guzman, Gaelen, Deik, Amy A., Pierce, Kerry A., Dennis, Courtney, Clish, Clary B., Carr, Steven A., Wagner, Bridget K., Schenone, Monica, Ng, Maggie C.Y., Chen, Brian H., Centeno-Cruz, Federico, Zerrweck, Carlos, Orozco, Lorena, Altshuler, David M., Schreiber, Stuart L., Florez, Jose C., Jacobs, Suzanne B. R., Lander, Eric S.
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2017
Gaiak:
Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC5562285/
https://ncbi.nlm.nih.gov/pubmed/28666119
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cell.2017.06.011
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