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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)

Se ha establecido un acuerdo interno que determina las responsabilidades respectivas de los responsables conjuntos del tratamiento, de conformidad con el artculo 26 del RGPD

Only one thing is certain at the moment, theyre not an instant cure for people living with obesity so its always worth talking to your GP for personalised care and advice

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