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

BACKGROUND: 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. METHODS: INS was sequenced in 116 maturity-onset diabetes of the young (MODYX) patients (n = 48 Danish and n...

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Bibliografski detalji
Glavni autori: Boesgaard, Trine W, Pruhova, Stepanka, Andersson, Ehm A, Cinek, Ondrej, Obermannova, Barbora, Lauenborg, Jeannet, Damm, Peter, Bergholdt, Regine, Pociot, Flemming, Pisinger, Charlotta, Barbetti, Fabrizio, Lebl, Jan, Pedersen, Oluf, Hansen, Torben
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2010
Teme:
Research Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC2848224/
https://ncbi.nlm.nih.gov/pubmed/20226046
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-11-42
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