Defective urinary carnitine transport in heterozygotes for primary carnitine deficiency
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical)
Reference24 articles.
1. Primary and secondary carnitine deficiency;Pons;J Child Neurol Suppl,1995
2. Primary carnitine deficiency due to a failure of carnitine transport in kidney, muscle, and fibroblasts;Treem;N Engl J Med,1988
3. Transport of carnitine into cells in hereditary carnitine deficiency;Eriksson;J Inherit Metab Dis,1989
4. Chronic cardiomyopathy and weakness or acute coma in children with a defect in carnitine uptake;Stanley;Ann Neurol,1991
5. Impaired skin fibroblast carnitine uptake in primary systemic carnitine deficiency manifested by childhood carnitine-responsive cardiomyopathy;Tein;Pediatr Res,1990
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