Patient with multiple acyl-CoA dehydrogenase deficiency disease and ETFDH mutations benefits from riboflavin therapy: a case report

Overview of attention for article published in BMC Medical Genomics, April 2018

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ETFDH #mutations https://t.co/wO6QuNpMI1 identified in #patients with multiple acyl-CoA dehydrogenase deficiency (MADD) #lipid #metabolic #disorder via #exome #sequencing https://t.co/fzgdDhzCUj

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