examine.com l-carnitine is Underrated. New Meta Review Reminds Us Why Celiac Disease: Symptoms, causes, treatments,

The gene encoding the human isoform of OCTN2 has been annotated and cloned in 1998, in parallel to the murine one (Tamai et al., 1998, 2000

CPT II deficiency (which most often presents with exercise intolerance and myoglobinuria and is discussed below) [130]

Metabolic interactions between peroxisomes and mitochondria with a special focus on acylcarnitine metabolism

L-carnitine: a partner between immune response and lipid metabolism

Tang NL, Ganapathy V, Wu X, Hui J, Seth P, Yuen PM, Wanders RJ, Fok TF, Hjelm NM: Mutations of OCTN2, an organic cation/carnitine transporter, lead to deficient cellular carnitine uptake in primary carnitine deficiency