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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Detalles Bibliográficos
Autores principales: 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
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2848224/
https://www.ncbi.nlm.nih.gov/pubmed/20226046
http://dx.doi.org/10.1186/1471-2350-11-42

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2848224/
https://www.ncbi.nlm.nih.gov/pubmed/20226046
http://dx.doi.org/10.1186/1471-2350-11-42

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