Hereditary defect in carnitine membrane transport is expressed in skin fibroblasts
- 1 August 1988
- journal article
- Published by Springer Nature in European Journal of Pediatrics
- Vol. 147 (6) , 662-668
- https://doi.org/10.1007/bf00442488
Abstract
No abstract availableKeywords
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- Systemic Carnitine Deficiency — A Treatable Inherited Lipid-Storage Disease Presenting as Reye's SyndromeNew England Journal of Medicine, 1980
- The syndrome of systemic carnitine deficiencyNeurology, 1975
- Carnitine Deficiency of Human Skeletal Muscle with Associated Lipid Storage Myopathy: A New SyndromeScience, 1973