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Published in 2018 at "Scientific Reports"
DOI: 10.1038/s41598-018-28314-z
Abstract: Wolfram syndrome (WS) is a rare autosomal recessive disorder caused by mutations in the WFS1 (Wolframin1) gene. The syndrome first manifests as diabetes mellitus, followed by optic nerve atrophy, deafness, and neurodegeneration. The underlying mechanism…
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Keywords:
glucose intolerance;
treatment;
wolfram syndrome;
development glucose ... See more keywords