KCNJ11 activating mutations in Italian patients with permanent neonatal diabetes.

Permanent neonatal diabetes mellitus (PNDM) is a rare condition characterized by severe hyperglycemia constantly requiring insulin treatment from its onset. Complete deficiency of glucokinase (GCK) can cause PNDM; however, the genetic etiology is unknown in most PNDM patients. Recently, heterozygous...

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Podrobná bibliografie
Hlavní autoři: Massa, O, Iafusco, D, D'Amato, E, Gloyn, A, Hattersley, A, Pasquino, B, Tonini, G, Dammacco, F, Zanette, G, Meschi, F, Porzio, O, Bottazzo, G, Crinó, A, Lorini, R, Cerutti, F, Vanelli, M, Barbetti, F
Médium: Journal article
Jazyk:English
Vydáno: 2005