Genetically induced dysfunctions of Kir2.1 channels: implications for short QT3 syndrome and autism–epilepsy phenotype

Elena Ambrosini(Istituto Superiore di Sanità), Mauro Pessia(Czech Academy of Sciences, Institute of Experimental Medicine), Renzo Guerrini(Meyer Children's Hospital), Carlo Napolitano(Agostino Gemelli University Polyclinic), Angela Lanciotti(Istituto Superiore di Sanità), Francesca Moro(Institute of Developmental Physiology), Paola Molinari(University of Sassari), Maria Stefania Brignone(Istituto Superiore di Sanità), Giulia Valvo(Fondazione Stella Maris), Stefania Pieroni(University of Perugia), Maria Cristina D’Adamo(Czech Academy of Sciences, Institute of Experimental Medicine), Ilenio Servettini(Czech Academy of Sciences, Institute of Experimental Medicine), Giuseppe Servillo(University of Perugia), Filippo M. Santorelli(Fondazione Stella Maris), Fabio Franciolini(University of Perugia), Federico Sicca(Fondazione Stella Maris), Alessandro Grottesi, Luca Guglielmi(University of Trento), Maria Marchese(Fondazione Stella Maris), Luigi Catacuzzeno(University of Perugia), Yanfei Ruan(Fondazione Salvatore Maugeri), Silvia G. Priori(University of Pavia)
Human Molecular Genetics
May 2, 2014
Cited by 85


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