l-carnitine deficiency in infants Exome sequencing identifies primary carnitine a family with cardiomyopathy and sudden death CARNITINE HOMEOSTASIS, MITOCHONDRIAL FUNCTION, AND

CARNITINE HOMEOSTASIS, MITOCHONDRIAL FUNCTION, AND CARDIOVASCULAR DISEASE PMC Neonatal Screening for Primary Carnitine Deficiency: Lessons Learned from the Faroe Islands Carnitine Transporter Deficiency Carnitine Deficiency Testing For Autism And Apraxia Increased detection of primary carnitine deficiency through second tier newborn genetic screening Orphanet Journal of Rare Diseases Springer Nature Link L Carnitine Linus Pauling Institute Oregon State University

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