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Ultrahigh-pressure liquid chromatography-mass spectrometry: An overview of the last decade
Importantly, any of the adverse events that were reported by patients were mild and no more prevalent or serious when compared to the group that received a placebo
doi: 10.1016/j.bbalip.2016.01.006
A.PloskerG
Pandey D , Agrawal S
mutations in OCTN2 lead to primary carnitine deficiency (PCD), a disorder characterized by systemic carnitine depletion and associated clinical manifestations, including muscle weakness, cardiomyopathy, and infertility
