l-carnitine deficiency in infants Exome sequencing identifies primary carnitine a family with cardiomyopathy and sudden death Increased detection of primary carnitine

Increased detection of primary carnitine deficiency through second tier newborn genetic screening Orphanet Journal of Rare Diseases Springer Nature Link Neonatal Screening for Primary Carnitine Deficiency: Lessons Learned from the Faroe Islands The Role of l Carnitine in Mitochondria, Prevention of Metabolic Inflexibility and Disease Initiation L Carnitine Linus Pauling Institute Oregon State University Carnitine Deficiency an overview ScienceDirect Topics

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