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Identification of an unusual variant peroxisome biogenesis disorder caused by mutations in the PEX16 gene
  1. Correspondence to Sacha Ferdinandusse, Laboratory Genetic Metabolic Diseases (F0-220), Academic Medical Centre, University of Amsterdam, Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands; s.ferdinandusse{at}amc.uva.nl
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Ebberink MS, Csanyi B, Chong WK, et al
Identification of an unusual variant peroxisome biogenesis disorder caused by mutations in the PEX16 gene

Publication history

  • Received October 19, 2009
  • Revised March 19, 2010
  • Accepted April 6, 2010
  • First published July 20, 2010.
Online issue publication 
April 27, 2016

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