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Waters Corporation, MA) using water with 0.1% formic acid (0.1% methanol and 5 mM ammonium acetate) detected with a Xevo-G2-QTOF MS (Waters Corporation) operating in a positive mode

Verbraucherzentrale NRW, Dsseldorf 2004, ISBN 3-933705-91-6

doi: 10.1126/science.182.4115.929

This article reviews and highlights special features about primary carnitine deficiency which is also commonly known as carnitine uptake defect (CUD)

Primary carnitine deficiency (PCD) is an autosomal recessive disorder characterized by a lack of plasma membrane carnitine transport owing to a shortcoming in the OCTN2 carnitine transporter