Lipid storage myopathy due to late-onset multiple Acyl-CoA dehydrogenase deficiency with novel mutations in ETFDH: A case report

Overview of attention for article published in Frontiers in Neurology, December 2022

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Lipid storage myopathy due to late-onset multiple Acyl-CoA dehydrogenase deficiency with novel mutations in ETFDH: A case report https://t.co/11PcU0leNi https://t.co/tAHv46UJ14

17 Dec 2022

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New Research: Lipid storage myopathy due to late-onset multiple Acyl-CoA dehydrogenase deficiency with novel mutations in ETFDH: A case report: Background Lipid storage myopathy (LSM) is an autosomal recessive inherited lipid and amino… https://t.co/4Xc26

15 Dec 2022

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