l carnitine for ms fatigue in Multiple Sclerosis: A Comprehensive Approach to E Comparison of short-term and long-term
Description
124 SloanJ
Carnitine metabolism and functions
mutations in OCTN2 lead to primary carnitine deficiency (PCD), a disorder characterized by systemic carnitine depletion and associated clinical manifestations, including muscle weakness, cardiomyopathy, and infertility
