APA

Ambrosini E., Sicca F., Brignone M. S., D'Adamo M. C., Napolitano C., Servettini I., Moro F., Ruan Y., Guglielmi L., Pieroni S., Servillo G., Lanciotti A., Valvo G., Catacuzzeno L., Franciolini F., Molinari P., Marchese M., Grottesi A., Guerrini R., Santorelli F. M., Priori S. & Pessia M. (20150423). Genetically induced dysfunctions of Kir2.1 channels: implications for short QT3 syndrome and autism-epilepsy phenotype. : Human molecular genetics.

Chicago

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 and Pessia Mauro. 20150423. Genetically induced dysfunctions of Kir2.1 channels: implications for short QT3 syndrome and autism-epilepsy phenotype. : Human molecular genetics.

Harvard

Ambrosini E., Sicca F., Brignone M. S., D'Adamo M. C., Napolitano C., Servettini I., Moro F., Ruan Y., Guglielmi L., Pieroni S., Servillo G., Lanciotti A., Valvo G., Catacuzzeno L., Franciolini F., Molinari P., Marchese M., Grottesi A., Guerrini R., Santorelli F. M., Priori S. and Pessia M. (20150423). Genetically induced dysfunctions of Kir2.1 channels: implications for short QT3 syndrome and autism-epilepsy phenotype. : Human molecular genetics.

MLA

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 and Pessia Mauro. Genetically induced dysfunctions of Kir2.1 channels: implications for short QT3 syndrome and autism-epilepsy phenotype. : Human molecular genetics. 20150423.