KCNJ11activating mutations in Italian patients with permanent neonatal diabetes

Human Mutation - Tập 25 Số 1 - Trang 22-27 - 2005
Ornella Massa1, Dario Iafusco2, Elena D’Amato3, Anna L. Gloyn4, Andrew T. Hattersley4, B Pasquino5, Giuseppe Tonini6, F Dammacco7, Giorgio Zanette8, Franco Meschi9, Ottavia Porzio10, G F Bottazzo1, Antonino Crinò1, Renata Lorini3, Fránco Cerutti11, Maurizio Vanelli12, Fabrizio Barbetti13,1
1Laboratory of Molecular Endocrinology and Metabolism, the Diabetes Unit, and the Scientific Directorate, Bambino Gesù Pediatric Hospital, Scientific Institute (IRCCS), Rome, Italy
2Department of Pediatrics, 2nd University of Naples, Naples, Italy
3Department of Pediatrics, University of Genoa, Genoa, Italy
4Institute of Biomedical and Clinical Science, Peninsula Medical School, Exeter, United Kingdom
5Department of Pediatrics, Regional Hospital, Bolzano, Italy
6Department of Pediatrics, Children Institute IRCCS "Burlo Garofolo," Trieste, Italy
7Division of Pediatric Endocrinology and Diabetes, Giovanni XXIII Hospital, Bari, Italy
8Diabetic Clinic, S. Maria degli Angeli, Pordenone, Italy
9Department of Pediatrics, Endocrine Unit, Scientific Institute H San Raffaele,Vita-Salute University, Milan, Italy
10Department of Internal Medicine, University of Rome ‘Tor Vergata’, Rome, Italy
11Department of Pediatrics, University of Turin, Turin, Italy
12Department of Pediatrics, University of Parma, Parma, Italy
13IBCIT, Biomedical Scientific Park of Rome S Raffaele, Rome, Italy

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