l carnitine deficiency radiology A novel pathogenic variant in the transporter gene, SLC22A5, in association with metabolic carnitine and cardiomyopathy features | BMC Cardiovascular Disorders Systemic Primary Carnitine Deficiency Presenting
Systemic Primary Carnitine Deficiency Presenting With Substantia Nigra and Basal Ganglia Injury: A Case Report Saito 2025 JIMD Reports Wiley Online Library Glutaric aciduria type 1 Radiology Reference Article Unmasking Primary Carnitine Deficiency as a Mimic of Hypertrophic Cardiomyopathy ScienceDirect Teaching NeuroImages: Glutaric aciduria type 1 (glutaryl CoA dehydrogenase deficiency) Neurology
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