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Ethylmalonic encephalopathy: Clinical course and therapy response in an uncommon mild case with a severe ETHE1 mutation - ScienceDirect
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Ethylmalonic encephalopathy and liver transplantation: long-term outcome of the first treated patient | Orphanet Journal of Rare Diseases | Full Text
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Figure 2 from Ethylmalonic-adipic aciduria. In vivo and in vitro studies indicating deficiency of activities of multiple acyl-CoA dehydrogenases. | Semantic Scholar
Hypoglycaemia and elevated urine ethylmalonic acid in a child homozygous for the shortâ•'chain acylâ•'CoA dehydrogenas
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