l carnitine cardiomyopathy Human model of primary deficiency reveals ferroptosis as a novel mechanism: Stem Cell Reports Exome sequencing identifies primary carnitine
Exome sequencing identifies primary carnitine deficiency in a family with cardiomyopathy and sudden death European Journal of Human Genetics The Role of L Carnitine in Kidney Disease and Related Metabolic Dysfunctions Role of carnitine in disease Nutrition & Metabolism Springer Nature Link Carnitine Deficiency an overview ScienceDirect Topics
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