Glucokinase (GCK) Mutations and Their Characterization in MODY2 Children of Southern Italy

Type 2 Maturity Onset Diabetes of the Young (MODY2) is a monogenic autosomal disease characterized by a primary defect in insulin secretion and hyperglycemia. It results from GCK gene mutations that impair enzyme activity. Between 2006 and 2010, we investigated GCK mutations in 66 diabetic children...

Descripción completa

Detalles Bibliográficos
Autores principales: Capuano, Marina, Garcia-Herrero, Carmen Maria, Tinto, Nadia, Carluccio, Carla, Capobianco, Valentina, Coto, Iolanda, Cola, Arturo, Iafusco, Dario, Franzese, Adriana, Zagari, Adriana, Navas, Maria Angeles, Sacchetti, Lucia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3385652/
https://www.ncbi.nlm.nih.gov/pubmed/22761713
http://dx.doi.org/10.1371/journal.pone.0038906

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3385652/
https://www.ncbi.nlm.nih.gov/pubmed/22761713
http://dx.doi.org/10.1371/journal.pone.0038906

Ejemplares similares