The first clinical case of a mutation at residue K185 of Kir6.2 (KCNJ11): a major ATP-binding residue. por Shimomura, K, de Nanclares, G, Foutinou, C, Caimari, M, Castaño, L, Ashcroft, F

Functional analysis of six Kir6.2 (KCNJ11) mutations causing neonatal diabetes. por Girard, C, Shimomura, K, Proks, P, Absalom, N, Castano, L, Perez de Nanclares, G, Ashcroft, F