Commentary: Neonatal onset in fatty acid oxidation disorders: How can we minimize morbidity and mortality?
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1005436414984/fullpdf
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3. Medium-chain acyl-CoA dehydrogenase defi ciency: Clinical course in 120 affected children;Iafolla;J Pediatr,1994
4. Common missense mutation G1528C in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. Characterization and expression of the mutant protein, mutation analysis on genomic DNA and chromosomal localization of the mitochondrial trifunctional protein alpha subunit gene;Ijlst;J Clin Invest,1996
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3. Disorders of Organic Acid Metabolism;Neurology of the Newborn;2008
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