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[DOI] [PMC free article] [PubMed] [Google Scholar] 35.Sekhar R.V., Patel S.G., Guthikonda A.P., Reid M., Balasubramanyam A., Taffet G.E., Jahoor F

One possible answer is that increased intracellular concentrations of either cation can lead to cellular hyperexcitability

Mutations in the major carnitine transporter, encoded by the SLC22A5 gene (also known as zwitterion/cation transporter 2 (OCTN2), are the predominant causes of primary carnitine deficiency (correctly identified as carnitine deficiency, systemic primary)

brenneri, C

Coat shine, comfortable skin, and strong, clean nails reflect a network fat quality, amino acids, micronutrients, hydration, and consistency

Z Gastroenterol