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Genetic and clinical aspects of Zellweger spectrum patients with PEX1 mutations
  1. Correspondence to:
 Dr Jutta Gärtner
 Department of Paediatrics and Paediatric Neurology, Georg August University, Robert-Koch-Strasse 40, 37075 Göttingen, Germany; gaertnjmed.uni-goettingen.de
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Citation

Rosewich H, Ohlenbusch A, Gärtner J
Genetic and clinical aspects of Zellweger spectrum patients with PEX1 mutations

Publication history

  • Received May 5, 2005
  • Accepted May 9, 2005
  • First published September 1, 2005.
Online issue publication 
September 01, 2005

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