Lactic acidosis in long-chain fatty acid β-oxidation disorders
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1005480516801/fullpdf
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4. Systems used for the transport of substrates into mitochondria;Chappell;Br Med Bull,1968
5. 3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective e.ect of medium-chain triglyceride treatment;Duran;Eur J Pediatr,1991
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