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A novel pathogenic variant in the carnitine transporter gene, SLC22A5, in association with metabolic carnitine deficiency and cardiomyopathy features BMC Cardiovascular Disorders Springer Nature Link Brain MRI Findings as an Important Diagnostic Clue in Glutaric Aciduria Type 1 PMC Typical imaging fi ndings in a 14 month old girl with Leigh syndrome Download Scientific Diagram Effect of l carnitine supplementation on muscle cramps induced by stroke: A case report ScienceDirect Brain MRI finding showed the T2 high, T1 low signal intensity single Download Scientific Diagram Primary carnitine deficiency cardiomyopathy International Journal of Cardiology
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