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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
- Source :
- Eiberg , H R L , Hansen , L , Kjer , B , Hansen , T , Pedersen , O , Bille , M , Rosenberg , T & Tranebjaerg , L 2006 , ' Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene ' , Journal of Medical Genetics , vol. 43 , no. 5 , pp. 435-440 .
- Publication Year :
- 2006
-
Abstract
- Udgivelsesdato: 2006/5
Details
- Database :
- OAIster
- Journal :
- Eiberg , H R L , Hansen , L , Kjer , B , Hansen , T , Pedersen , O , Bille , M , Rosenberg , T & Tranebjaerg , L 2006 , ' Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene ' , Journal of Medical Genetics , vol. 43 , no. 5 , pp. 435-440 .
- Notes :
- English
- Publication Type :
- Electronic Resource
- Accession number :
- edsoai.ocn889771307
- Document Type :
- Electronic Resource