Citation Tools

Download PDFPDF
Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene

Download to a citation manager

Cite this article as:
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