US$ 24.06
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

Ingredients: L-carnitine tartrate, anti-caking agents (E341, E470b, E551)

During data analysis, to be consistent with the convention where larger values reflect increasing symptom severity, the raw score axis was flipped ( i.e

doi: 10.1111/cas.12904 312 ZhuH.WuH.LiuX

FSGS: Focal segmental glomerulosclerosis
