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Heterozygous truncating mutation in the human homeobox gene GSH2 has no discernable phenotypic effect
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  1. Correspondence to:
 Dr D J M Peters, Center of Human and Clinical Genetics, Leiden University Medical Centre, Sylvius Laboratory, Wassenaarseweg 72, 2333AL Leiden, The Netherlands;
 d.j.m.peters{at}lumc.nl
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Citation

Dauwerse JG, de Die-Smulders CEM, Bakker E, et al
Heterozygous truncating mutation in the human homeobox gene GSH2 has no discernable phenotypic effect

Publication history

  • First published September 1, 2002.
Online issue publication 
September 01, 2002

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