l-carnitine deficiency in infants Frontiers Exome sequencing identifies primary carnitine
Exome sequencing identifies primary carnitine deficiency in a family with cardiomyopathy and sudden death European Journal of Human Genetics Newborn screening for primary carnitine deficiency: who will benefit? a retrospective cohort study Journal of Medical Genetics Role of carnitine in disease Nutrition & Metabolism Springer Nature Link Carnitine Deficiency MD Searchlight
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