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One or more keywords matched the following properties of Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico.
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has major subject area list Diabetes Mellitus, Type 2; Genetic Predisposition to Disease; Monocarboxylic Acid Transporters; Polymorphism, Single Nucleotide
has minor subject area list African Continental Ancestry Group; Alleles; Animals; Asian Continental Ancestry Group; Cohort Studies; Endoplasmic Reticulum; European Continental Ancestry Group; Female; Genome-Wide Association Study; Haplotypes; HeLa Cells; Humans; Indians, North American; Lipid Metabolism; Liver; Male; Mexico; Neanderthals; RNA, Messenger; Triglycerides
information resource reference Williams AL, Jacobs SB, Moreno-Macías H, Huerta-Chagoya A, Churchhouse C, Márquez-Luna C, García-Ortíz H, Gómez-Vázquez MJ, Burtt NP, Aguilar-Salinas CA, González-Villalpando C, Florez JC, Orozco L, Haiman CA, Tusié-Luna T, Altshuler D. Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico. Nature. 2014 Feb 06; 506(7486):97-101.
label Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico.
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