Evidence for autosomal recessive inheritance in systemic carnitine deficiency
- 1 February 1982
- journal article
- case report
- Published by Wiley in Annals of Neurology
- Vol. 11 (2) , 190-192
- https://doi.org/10.1002/ana.410110214
Abstract
No abstract availableKeywords
This publication has 6 references indexed in Scilit:
- Systemic Carnitine Deficiency — A Treatable Inherited Lipid-Storage Disease Presenting as Reye's SyndromeNew England Journal of Medicine, 1980
- Disorders of lipid metabolism in muscleMuscle & Nerve, 1980
- Carnitine-induced uptake of l-carnitine into cells from an established cell line from human heart (CCL 27)Biochimica et Biophysica Acta (BBA) - Biomembranes, 1978
- Carnitine deficiency: clinical, morphological, and biochemical observations in a fatal case.Journal of Neurology, Neurosurgery & Psychiatry, 1977
- Fatal cases of lipid storage myopathy with carnitine deficiency.Journal of Neurology, Neurosurgery & Psychiatry, 1977
- Role of carnitine in hepatic ketogenesis.Proceedings of the National Academy of Sciences, 1975