DIHEXA - Research Grade Peptide
US$ 23.02
wirkung von l-carnitin : auf den menschlichen Körper L-Carnitin | SW10013
Description
The CACT Deficiency Disorder is caused by mutations in the SLC25A20 gene Treatment is done by avoiding fasting and having a low long-chain fat diet with medium chain triglyceride (MCT) supplementation (Source: Carnitine-Acylcarnitine Translocase Deficiency
doi: 10.30744/brjac.2179-3425.2018.5.20.9-11
[DOI] [PubMed] [Google Scholar] 38.Derosa G., Maffioli P., Salvadeo S.A., Ferrari I., Gravina A., Mereu R., DAngelo A., Palumbo I., Randazzo S., Cicero A.F
10.1016/j.juro.2008.01.093 22 DellH.RochaJ
En savoir plus Tartrate de L-carnitine complment alimentaire Carnipure
