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First PEX11β patient extends spectrum of peroxisomal biogenesis disorder phenotypes
  1. Correspondence to Dr S Thoms, Department of Pediatrics and Pediatric Neurology, University Medical Center Göttingen, University of Göttingen, Robert Koch Strasse 40, 37075 Göttingen, Germany; sven.thoms{at}med.uni-goettingen.de
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Citation

Thoms S, Gärtner J
First PEX11β patient extends spectrum of peroxisomal biogenesis disorder phenotypes

Publication history

  • Received March 19, 2012
  • Accepted April 3, 2012
  • First published May 11, 2012.
Online issue publication 
May 11, 2012

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