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Description
Writing-original draft preparation: A.S., G.R

Rare mutations in the SLC22A5 gene can cause a genetic condition called primary carnitine deficiency, which is usually discovered in infancy because it affects brain function, muscle function, and blood glucose levels

Das sorgt fr mehr Energie im Alltag, effektivere Fettverbrennung und ein gesundes Herz-Kreislauf-System

Mitsumoto M, Cassens RG, Schaefer DM, Scheller KK
