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A fatal case of neonatal onset multiple acyl-CoA dehydrogenase deficiency caused by novel mutation of ETFDH gene: case report https://t.co/6xxs1VT6yR https://t.co/RR8kupsolO
A fatal case of neonatal onset multiple acyl-CoA dehydrogenase deficiency caused by novel mutation of ETFDH gene: case report https://t.co/6xxs1VT6yR https://t.co/RR8kupsolO
RT @IronBiologyBot: A fatal case of neonatal onset multiple acyl-CoA dehydrogenase deficiency caused by novel mutation of ETFDH gene: case…
A fatal case of neonatal onset multiple acyl-CoA dehydrogenase deficiency caused by novel mutation of ETFDH gene: case report https://t.co/WXBJE4Sc6u #IronBiology #BioIron #Iron