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Genetically induced dysfunctions of Kir2.1 channels: implications for short QT3 syndrome and autism-epilepsy phenotype.
Ambrosini, Elena; Sicca, Federico; Brignone, Maria S; D'Adamo, Maria C; Napolitano, Carlo; Servettini, Ilenio; Moro, Francesca; Ruan, Yanfei; Guglielmi, Luca; Pieroni, Stefania; Servillo, Giuseppe; Lanciotti, Angela; Valvo, Giulia; Catacuzzeno, Luigi; Franciolini, Fabio; Molinari, Paola; Marchese, Maria; Grottesi, Alessandro; Guerrini, Renzo; Santorelli, Filippo M; Priori, Silvia; Pessia, Mauro.
Afiliación
  • Ambrosini E; Department of Cell Biology and Neuroscience, Istituto Superiore di Sanità, Viale Regina Elena 299, Rome 00161, Italy, elena.ambrosini@iss.it.
  • Sicca F; Clinical Neurophysiology Laboratory, Department of Developmental Neuroscience and.
  • Brignone MS; Department of Cell Biology and Neuroscience, Istituto Superiore di Sanità, Viale Regina Elena 299, Rome 00161, Italy.
  • D'Adamo MC; Faculty of Medicine, Section of Physiology & Biochemistry, Department of Experimental Medicine.
  • Napolitano C; Molecular Cardiology, IRCCS Salvatore Maugeri Foundation, Pavia, Italy.
  • Servettini I; Faculty of Medicine, Section of Physiology & Biochemistry, Department of Experimental Medicine.
  • Moro F; Clinical Neurophysiology Laboratory, Department of Developmental Neuroscience and.
  • Ruan Y; Molecular Cardiology, IRCCS Salvatore Maugeri Foundation, Pavia, Italy.
  • Guglielmi L; Faculty of Medicine, Section of Physiology & Biochemistry, Department of Experimental Medicine.
  • Pieroni S; Faculty of Medicine, Department of Experimental Medicine and.
  • Servillo G; Faculty of Medicine, Department of Experimental Medicine and.
  • Lanciotti A; Department of Cell Biology and Neuroscience, Istituto Superiore di Sanità, Viale Regina Elena 299, Rome 00161, Italy.
  • Valvo G; Clinical Neurophysiology Laboratory, Department of Developmental Neuroscience and.
  • Catacuzzeno L; Department of Chemistry, Biology and Biotechnology, University of Perugia, Perugia, Italy.
  • Franciolini F; Department of Chemistry, Biology and Biotechnology, University of Perugia, Perugia, Italy.
  • Molinari P; Department of Pharmacology, Istituto Superiore di Sanità, Rome, Italy.
  • Marchese M; Molecular Medicine Laboratory, IRCCS Stella Maris Foundation, Pisa, Italy.
  • Grottesi A; Computational Medicine and Biology Group, CASPUR, Rome, Italy and.
  • Guerrini R; Clinical Neurophysiology Laboratory, Department of Developmental Neuroscience and Pediatric Neurology Unit and Laboratories, Children's Hospital A. Meyer-University of Florence, Florence, Italy.
  • Santorelli FM; Molecular Medicine Laboratory, IRCCS Stella Maris Foundation, Pisa, Italy.
  • Priori S; Molecular Cardiology, IRCCS Salvatore Maugeri Foundation, Pavia, Italy.
  • Pessia M; Faculty of Medicine, Section of Physiology & Biochemistry, Department of Experimental Medicine.
Hum Mol Genet ; 23(18): 4875-86, 2014 Sep 15.
Article en En | MEDLINE | ID: mdl-24794859
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Arritmias Cardíacas / Trastorno Autístico / Canales de Potasio de Rectificación Interna / Epilepsia / Sistema de Conducción Cardíaco / Cardiopatías Congénitas Límite: Animals / Child / Humans / Male Idioma: En Año: 2014 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Arritmias Cardíacas / Trastorno Autístico / Canales de Potasio de Rectificación Interna / Epilepsia / Sistema de Conducción Cardíaco / Cardiopatías Congénitas Límite: Animals / Child / Humans / Male Idioma: En Año: 2014 Tipo del documento: Article