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 |
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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