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POMGnT1 mutation and phenotypic spectrum in muscle-eye-brain disease
  1. Correspondence to:
 Dr Anna-Elina Lehesjoki
 Folkhälsan Institute of Genetics, Biomedicum Helsinki, PO Box 63 (Haartmaninkatu 8), FIN-00014 University of Helsinki, Finland; anna-elina.lehesjokihelsinki.fi
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Citation

Diesen C, Saarinen A, Pihko H, et al
POMGnT1 mutation and phenotypic spectrum in muscle-eye-brain disease

Publication history

  • First published October 1, 2004.
Online issue publication 
April 27, 2016

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