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Literature summary for
1.5.5.1
extracted from
Spaan, AN; Ijlst, L; van Roermund, CW; Wijburg, FA; Wanders, RJ; Waterham, HR
Identification of the human mitochondrial FAD transporter and its potential role in multiple acyl-CoA dehydrogenase deficiency.
(2005),
Mol Genet Metab
, 86, 441-7.
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