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Description
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

& Arezzo, J

The Acute Toxicity of Choline Hydrochloride in Mice and Rats
Electromyography (EMG) Tests electrical activity in muscles

Mol Psychiatry 2022:1 [DOI] [PMC free article] [PubMed] [Google Scholar] 136.Tsai SY, Chen HJ, Chen C, Lio CF, Kuo CF, Leong KH, Wang YT, Yang TY, You CH, Wang WS (2019) Increased risk of chronic fatigue syndrome following psoriasis: a nationwide population-based cohort study