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Description
Mutations in CPT1 can cause carnitine palmitoyltransferase I (CPT I) deficiency, which is an autosomal recessive genetic condition (need two copies of the mutation)
ALCAR belongs to that same system but as a short-chain acylcarnitine
Flanagan, P.A
See more No, intravenous iron dextran is not considered a prohibited plasma expander
Bipolar disorder and valproate-induced hyperammonemic encephalopathy in an adolescent with diabetes
Eur Heart J Cardiovasc Imaging
