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Description
Samples of culture supernatant quenched by addition of formic acid to a final concentration of 0.1% were analyzed by LC-MS/MS to quantify concentrations of d 9 -TMA, d 9 -l-carnitine, and/or d 9 -BB
Primary carnitine deficiency is a genetic disorder of the cellular carnitine-transporter system that typically appears by the age of five with symptoms of cardiomyopathy, skeletal-muscle weakness, and hypoglycemia
L-Carnitine 500 is non-hormonal and does not suppress natural testosterone
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