l carnitine deficiency radiology A novel pathogenic variant in the transporter gene, SLC22A5, in association with metabolic carnitine and cardiomyopathy features | BMC Cardiovascular Disorders MRI Findings in Encephalopathy with
MRI Findings in Encephalopathy with Primary Carnitine Deficiency: A Case Report Yilmaz 2015 Journal of Neuroimaging Wiley Online Library Glutaric aciduria type 1 Radiology Reference Article Primary carnitine deficiency cardiomyopathy International Journal of Cardiology Unmasking Primary Carnitine Deficiency as a Mimic of Hypertrophic Cardiomyopathy ScienceDirect
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