Isobutyryl-CoA dehydrogenase deficiency associated with autism in a girl without an alternative genetic diagnosis by trio whole exome sequencing: A case report
M. Eleftheriadou, E. Medici-van den Herik, K. Stuurman, Y. van Bever, D.M.E.I. Hellebrekers, M. van Slegtenhorst, G. Ruijter, T.S. Barakat*
Research output: Contribution to journal › Article › Academic › peer-review
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