Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY)
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
Insulin gene (INS) mutations have recently been described as a common cause of permanent neonatal diabetes (PNDM) and a rare cause of diabetes diagnosed in childhood or adulthood.
| Originalsprog | Engelsk |
|---|---|
| Tidsskrift | B M C Medical Genetics |
| Vol/bind | 11 |
| Sider (fra-til) | 42 |
| ISSN | 1471-2350 |
| DOI | |
| Status | Udgivet - 1 jan. 2010 |
ID: 34076391