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PMID: 18449137 [PubMed] [Google Scholar] [220].Skalny AV, Skalnaya MG, Grabeklis AR, Skalnaya AA, Tinkov AA

Molecular Biology of Primary Carnitine Deficiency The SLC22A5 (OCTN2) gene is located on chromosome 5q31.1 and is composed of 11 exons that generate two alternatively spliced mRNAs encoding proteins of 581 amino acids (isoform a) and 557 amino acids (isoform b)

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For individuals looking to improve exercise variables and performance via the use of L-carnitine supplementation, chronic L-carnitine and carbohydrate intake is a better method to increase the content of L-carnitine in skeletal muscle and to influence performance (31)

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