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ETFDH mutations as a major cause of riboflavin-responsive... | ResearchHub
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ETFDH mutations as a major cause of riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency
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Authors
Rikke Olsen
15 more
Rikke Olsen
•
John Dean
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•
Andrew Morris
Published
June 22, 2007
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Journal
Brain
Topics
Biology
Biochemistry
Chemistry
Clinical Biochemistry
Molecular Biology
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DOI
10.1093/brain/awm135
