Endocardial fibroelastosis and primary carnitine deficiency due to a defect in the plasma membrane carnitine transporter
Author:
Publisher
Wiley
Subject
Cardiology and Cardiovascular Medicine,General Medicine
Reference14 articles.
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2. Fatty acid oxidation disorders: A new class of metabolic diseases;Hale;J Pediatr,1992
3. Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptake;Stanley;Ann Neurol,1991
4. Hypoglycemia, hypotonia and cardiomyopathy: The evolving clinical picture of long-chain acyl-CoA dehydrogenase deficiency;Treem;Pediatrics,1991
5. Long-chain 3-hydroxacyl-CoA dehydrogenase deficiency: Identification of a new inborn error of mitochondrial fatty acid p-oxidation;Wanders;J Inker Metab Dis,1990
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