l carnitine deficiency radiology A novel pathogenic variant in the transporter gene, SLC22A5, in association with metabolic carnitine and cardiomyopathy features | BMC Cardiovascular Disorders Experimental and Therapeutic Medicine
Experimental and Therapeutic Medicine Unmasking Primary Carnitine Deficiency as a Mimic of Hypertrophic Cardiomyopathy ScienceDirect Effect of l carnitine supplementation on muscle cramps induced by stroke: A case report ScienceDirect Getting the diagnostic clue, role of MRI in the diagnosis of type 1 Glutaric aciduria in resource limited settings ScienceDirect
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