Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction.
- Published in:
- Nature Genetics, 2006, v. 38, n. 1, p. 54, doi. 10.1038/ng1708
- By:
- Publication type:
- Article
Works matching AU Eide, Stig Å
Results: 3
1
2
Familial occurrence of neonatal diabetes with duplications in chromosome 6q24: treatment with sulfonylurea and 40-yr follow-up.
- Published in:
- Pediatric Diabetes, 2012, v. 13, n. 2, p. 155, doi. 10.1111/j.1399-5448.2011.00776.x
- By:
- Publication type:
- Article
3
Studies in 3,523 Norwegians and Meta-Analysis in 11,571 Subjects Indicate That Variants in the Hepatocyte Nuclear Factor 4α (HNF4A) P2 Region Are Associated With Type 2 Diabetes in Scandinavians.
- Published in:
- Diabetes, 2007, v. 56, n. 12, p. 3112, doi. 10.2337/db07-0513
- By:
- Publication type:
- Article