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Mutations in the major carnitine transporter, encoded by the SLC22A5 gene (also known as organic zwitterion/cation transporter 2 (OCTN2), are the predominant causes of primary carnitine deficiency (correctly identified as carnitine deficiency, systemic primary)
Explore the spectrum of B12 solutions beyond the needle with our comprehensive guide, B12 Shots & B12 Injections: The Good, Bad and Alternative! Discover the effectiveness and convenience of vit B12 injection alternatives, offering the same benefits in non-invasive forms like patches or oral supplements for your health journey
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