Finnish-specific AKT2 gene variant leads to impaired insulin signalling in myotubes
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DOI: 10.1530/jme-21-0285
Abstract: Finnish-specific gene variant p.P50T/AKT2 (minor allele frequency (MAF) = 1.1%) is associated with insulin resistance and increased predisposition to type 2 diabetes. Here, we have investigated in vitro the impact of the gene variant on glucose metabolism… read more here.
Keywords: finnish specific; insulin stimulated; akt2; gene variant ... See more keywords