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cpt ii deficiency
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CPT2
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
Novel mutations associated with carnitine palmitoyltransferase II deficiency
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