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Why screen newborns for profound and partial biotinidase deficiency?

Barry Wolf1

  • 1Department of Research Administration, Henry Ford Hospital, Detroit, MI 48202, USA; Center for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, MI 48201, USA.

Molecular Genetics and Metabolism
|February 2, 2015
PubMed
Summary

No abstract available in PubMed .

Keywords:
BiotinidaseBiotinidase deficiencyNewborn screeningPartial biotinidase deficiencyProfound biotinidase deficiencyScreening

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