cardiomyopathy l-carnitine Metabolic therapy for cardiovascular diseases with propionyl Exome sequencing identifies primary carnitine
Exome sequencing identifies primary carnitine deficiency in a family with cardiomyopathy and sudden death European Journal of Human Genetics Human model of primary carnitine deficiency cardiomyopathy reveals ferroptosis as a novel mechanism ScienceDirect The Role of L Carnitine in Kidney Disease and Related Metabolic Dysfunctions Carnitine Supplementation in Chronic Hemodialysis PatientsA Literature Review
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