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Identification of an unusual variant peroxisome biogenesis disorder caused by mutations in the PEX16 gene
- 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
Citation
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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© 2010, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions.