Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene
Research output: Contribution to journal › Journal article › Research › peer-review
Udgivelsesdato: 2006/5
| Original language | English |
|---|---|
| Journal | Journal of Medical Genetics |
| Volume | 43 |
| Issue number | 5 |
| Pages (from-to) | 435-440 |
| Number of pages | 5 |
| ISSN | 1468-6244 |
| Publication status | Published - 2006 |
ID: 1200318