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Elsevier, Molecular Genetics and Metabolism, 4(122), p. 182-188, 2017

DOI: 10.1016/j.ymgme.2017.10.014

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An intronic variation in SLC52A1 causes exon skipping and transient riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency

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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