Sudden neonatal death in carnitine transporter deficiency
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference11 articles.
1. Primary carnitine deficiency due to a failure of carnitine transport in kidney, muscle, and fibroblasts;Treem;N Engl J Med,1988
2. A genetic defect in carnitine transport causing primary carnitine deficiency;Stanley;Progr Clin Biol Res,1990
3. Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptake;Stanley;Ann Neurol,1991
4. Biochemical diagnosis of fatty acid oxidation disorders by metabolite analysis of postmortem liver;Boles;Hum Pathol,1994
5. Endocardial fibroelastosis and primary carnitine deficiency due to a defect in the plasma membrane carnitine transporter;Bennett;Clin Cardiol,1996
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