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cpt deficiency, hepatic, type ii
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CPT2
Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library
Two CPT2 mutations in three Japanese patients with carnitine palmitoyltransferase II deficiency: functional analysis and association with polymorphic haplotypes and two clinical phenotypes
Identification of four novel mutations in patients with carnitine palmitoyltransferase II (CPT II) deficiency
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