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Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene
  1. Correspondence to:
 Dr H Eiberg
 Department of Medical Biochemistry and Genetics, Section G, Panum Institute, University of Copenhagen, Blegdamsvej 3b, DK-2200 Copenhagen N, Denmark; he{at}imbg.ku.dk
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Citation

Eiberg H, Hansen L, Kjer B, et al
Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene

Publication history

  • Received May 13, 2005
  • Accepted September 6, 2005
  • Revised August 19, 2005
  • First published April 28, 2006.
Online issue publication 
April 28, 2006

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