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 Carnitine and acylcarnitine levels in infants with primary carnitine Download Scientific Diagram What are the symptoms of carnitine (L carnitine) deficiency? Role of carnitine in disease Nutrition & Metabolism Springer Nature Link
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