Carnitine palmitoyltransferase II (CPT II) deficiency: Genotype–Phenotype analysis of 50 patients
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
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4. Infantile form of carnitine palmitoyltransferase II deficiency with hepatomuscular symptoms and sudden death. Physiological approach to carnitine palmitoyltransferase II deficiencies;Demaugre;J Clin Invest,1991
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