l carnitine india review GAT 60vc | Buy at Kiwla Buy User's Guide to Carnitine

Primary carnitine deficiency is a genetic disorder of the cellular carnitine delivery system that typically manifests around the age of five with symptoms of cardiomyopathy, skeletal muscle weakness and hypoglycemia

Appl Environ Microbiol 68, 47104716

The compound helps improve memory and learning ability by increasing the production of acetylcholine, a neurotransmitter that is important for cognitive function

Here's why

The disease is characterized by general metabolic derangement, cardiomyopathy, hyperammonemia, hypoglycemia, muscle weakness, and myopathy, in line with the crucial role of carnitine in FAO (Nezu et al., 1999)