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The influence of the ketogenic diet on the therapy of type 2 diabetes
doi: 10.1038/s42003-021-01741-x 11 RiquelmeEZhangYZhangLMontielMZoltanMDongWet al
Bazzone et al., 2016, 2017)
SLC22A5 mutations impair OCTN2 function, causing primary carnitine deficiency (PCD) (1517), an autosomal recessive disorder characterized by skeletal myopathy, progressive cardiomyopathy, hypoglycemia, and hyperammonemia
Peyronies Disease: A Guide to Clinical Management
