Found: 4
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Association studies of genetic variation in the WFS1 gene and type 2 diabetes in U.K. populations.
- Published in:
- 2002
- By:
- Publication type:
- journal article
Homozygous Mutations in NEUROD1 Are Responsible for a Novel Syndrome of Permanent Neonatal Diabetes and Neurological Abnormalities.
- Published in:
- Diabetes, 2010, v. 59, n. 9, p. 2326, doi. 10.2337/db10-0011
- By:
- Publication type:
- Article
Wolcott-Rallison syndrome is the most common genetic cause of permanent neonatal diabetes in consanguineous families.
- Published in:
- 2009
- By:
- Publication type:
- journal article
Characterization of [<sup>125</sup>I]-SB-258585 binding to human recombinant and native 5-HT<sub>6</sub> receptors in rat, pig and human brain tissue.
- Published in:
- British Journal of Pharmacology, 2000, v. 130, n. 7, p. 1597, doi. 10.1038/sj.bjp.0703458
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- Publication type:
- Article