Dietary management of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD). A case report and survey
Author:
Affiliation:
1. ; The Biochemical Genetics Program, Waisman Center, Department of Pediatrics; University of Wisconsin - Madison; Madison Wisconsin USA; and
2. ; The Department of Nutritional Sciences; University of Wisconsin - Madison; Madison Wisconsin USA
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1005437616934/fullpdf
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4. Very long chain acyl-CoA dehydrogenase deficiency: successful treatment of acute cardiomyopathy;Brown-Harrison;Biochem Mol Med,1996
5. Dietary e.ects on brain fatty acid composition: the reversibility of n-3 fatty acid deficiency and turnover of docosahexaenoic acid in the brain, erythrocytes, and plasma of rhesus monkeys;Connor;J Lipid Res,1990
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