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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)

Men who experience sudden onset erectile dysfunction (ED), especially after age 50, may have underlying cardiovascular disease, and it can be an early warning sign of serious health problems that requires urgent evaluation

Working group for developing the guidelines for parenteral nutrition of The German Association for Nutritional Medicine

Metabolische Flexibilitt Um an Energie zu kommen, knnen Deine Zellen stets zwischen Fetten und Kohlenhydraten entscheiden

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GSEA 55,56 was performed by comparing DKO cells to all other genotypes combined (WT, ACLY KO, ACSS2 KO)