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WFS1, (dbSNP rs6446482)
National Institutes of Health
Semantic Scholar uses AI to extract papers important to this topic.
Association study of the effect of WFS1 polymorphisms on risk of type 2 diabetes in Japanese population.
The Kobe journal of medical sciences
Corpus ID: 26035557
Mutations of WFS1 gene cause Wolfram syndrome, which is a rare autosomal recessive disorder characterized by juvenile diabetes…
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