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Primary carnitine deficiency (PCD) is an autosomal recessive disorder of mitochondrial -oxidation resulting from defective carnitine transport and is one of the rare treatable etiologies of metabolic cardiomyopathies
Watch this space, Dr
Transl Research
Fiati Kenston SS, Song X, Li Z, Zhao J (2019) Mechanistic insight, diagnosis, and treatment of ammonia-induced hepatic encephalopathy
And you can come out the other side of anything.
Scientific Reports, 6, 37664
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