l carnitine cardiomyopathy Cardiac function and incidence of unexplained myocardial scarring in patients with primary deficiency - a cardiac magnetic resonance study Human model of primary carnitine
Human model of primary carnitine deficiency cardiomyopathy reveals ferroptosis as a novel mechanism: Stem Cell Reports Exome sequencing identifies primary carnitine deficiency in a family with cardiomyopathy and sudden death European Journal of Human Genetics Hong Kong Journal of Paediatrics [HK J Paediatr (New Series) 2020;25:23 29] Carnitine Deficiency: What You Need to Know The Medical Biochemistry Page
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