l-carnitine deficiency in infants Exome sequencing identifies primary carnitine a family with cardiomyopathy and sudden death Role of carnitine in disease
Role of carnitine in disease Nutrition & Metabolism Springer Nature Link Carnitine Deficiency Testing For Autism And Apraxia Carnitine Transporter Deficiency Increased detection of primary carnitine deficiency through second tier newborn genetic screening Orphanet Journal of Rare Diseases Springer Nature Link SPCD Treatment Guide: L Carnitine & Crises Inciteful Med Resources
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