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...

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Detaylı Bibliyografya
Asıl Yazarlar: 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
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Public Library of Science 2012
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3385652/
https://ncbi.nlm.nih.gov/pubmed/22761713
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0038906
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