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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
- 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
Citation
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 27, 2016
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Copyright 2006 Journal of Medical Genetics