Research map: Cardiac MRI reveals myocardial fibrosis and systolic dysfunction in mitochondrial trifunctional protein–deficient mice

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  20. 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. · Lodewijk IJlst · 1996 · 168 citations · Cited by this paper
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  31. Clinical and biological features at diagnosis in mitochondrial fatty acid beta‐oxidation defects: a French pediatric study from 187 patients. Complementary data · Julien Baruteau · 2013 · 50 citations · Cited by this paper
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