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July 1, 1998Annual Review of Nutrition

Genetic Disorders of Carnitine Metabolism and Their Nutritional Management

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Authors

JKJános KernerPoznan University of Medical SciencesCHCharles L. HoppelPennington Biomedical Research Center

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Kerner et al. (1998) studied this question.

synapsesocial.com/papers/6a740a618ab8a3dde2eafd29https://doi.org/10.1146/annurev.nutr.18.1.179
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Also Consider

Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Carnitine--metabolism and functions1983 · 1,690 citations
  2. 2Skin fibroblast carnitine uptake in secondary carnitine deficiency disorders1991 · 12 citations
  3. 3Observations on the affinity for carnitine, and malonyl-CoA sensitivity, of carnitine palmitoyltransferase I in animal and human tissues. Demonstration of the presence of malonyl-CoA in non-hepatic tissues of the rat1983 · 558 citations
  4. 4Plasma and muscle free carnitine deficiency due to renal Fanconi syndrome.1985 · 119 citations