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Primary systemic carnitine deficiency Primary systemic carnitine deficiency is a rare, autosomal recessive disorder caused by mutations (including deletions) in the SLC22A5 gene coding for carnitine transporter protein OCTN2 (organic cation transporter novel 2) (33)
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Whats inside Partial disclosure Nerve Shield contains ten active ingredients
- Immune Support: Strengthens the immune system by protecting cells from damage and supporting overall immune function
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