Structure—function analysis of the α5 and the α13 helices of human glucokinase: Description of two novel activating mutations

Por Pedelini, Leda, Garcia-Gimeno, Maria Adelaida, Marina, Alberto, Gomez-Zumaquero, Juan M., Rodriguez-Bada, Pablo, López-Enriquez, Soledad, Soriguer, Federico C., Cuesta-Muñoz, Antonio L., Sanz, Pascual
Publicado em 2005

Clinical Heterogeneity in Monogenic Diabetes Caused by Mutations in the Glucokinase Gene (GCK-MODY)

Por Cuesta-Muñoz, Antonio L., Tuomi, Tiinamaija, Cobo-Vuilleumier, Nadia, Koskela, Hanna, Odili, Stella, Stride, Amanda, Buettger, Carol, Otonkoski, Timo, Froguel, Philippe, Grimsby, Joseph, Garcia-Gimeno, Maria, Matschinsky, Franz M.
Publicado em 2010

Opposite Clinical Phenotypes of Glucokinase Disease: Description of a Novel Activating Mutation and Contiguous Inactivating Mutations in Human Glucokinase (GCK) Gene

Por Barbetti, Fabrizio, Cobo-Vuilleumier, Nadia, Dionisi-Vici, Carlo, Toni, Sonia, Ciampalini, Paolo, Massa, Ornella, Rodriguez-Bada, Pablo, Colombo, Carlo, Lenzi, Lorenzo, Garcia-Gimeno, María A., Bermudez-Silva, Francisco J., Rodriguez de Fonseca, Fernando, Banin, Patrizia, Aledo, Juan C., Baixeras, Elena, Sanz, Pascual, Cuesta-Muñoz, Antonio L.
Publicado no Mol Endocrinol (2009)