Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY)

Research output: Contribution to journalJournal articleResearchpeer-review

Trine W Boesgaard, Stepanka Pruhova, Ehm A Andersson, Ondrej Cinek, Barbora Obermannova, Jeannet Lauenborg, Peter Damm, Regine Bergholdt, Flemming Pociot, Charlotta Pisinger, Fabrizio Barbetti, Jan Lebl, Oluf Pedersen, Torben Hansen

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.
Original languageEnglish
JournalB M C Medical Genetics
Volume11
Pages (from-to)42
ISSN1471-2350
DOIs
Publication statusPublished - 1 Jan 2010

    Research areas

  • Diabetes Mellitus, Type 1, Diabetes Mellitus, Type 2, Diabetes, Gestational, Female, Genetic Variation, Humans, Insulin, Male, Mutation, Pedigree, Phenotype, Pregnancy, Young Adult

ID: 34076391