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Cardiac function and incidence of unexplained myocardial scarring in patients with primary carnitine deficiency a cardiac magnetic resonance study Scientific Reports Frontiers Case report: Mitochondrial trifunctional protein deficiency caused by HADHB gene mutation (c.1175C>T) characterized by higher brain dysfunction followed by neuropathy, presented gadolinium enhancement on brain imaging in an adult patient Glutaric aciduria type 1 Radiology Reference Article Brain MRI Findings as an Important Diagnostic Clue in Glutaric Aciduria Type 1 PMC MR Neuroimaging in Pediatric Inborn Errors of Metabolism

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