Published in

Wiley, Clinical Genetics, 2(87), p. 196-198, 2014

DOI: 10.1111/cge.12350

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A novel ACAD8 mutation in asymptomatic patients with isobutyryl-CoA dehydrogenase deficiency and a review of the ACAD8 mutation spectrum : Letter to the Editor

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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