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cpt ii deficiency, lethal neonatal
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CPT2
Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides
Identification of a common mutation in the carnitine palmitoyltransferase II gene in familial recurrent myoglobinuria patients
Two novel sequence polymorphisms of the human carnitine palmitoyltransferase II (CPT1) gene
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