Genetically induced dysfunctions of Kir2.1 channels: implications for short QT3 syndrome and autism-epilepsy phenotype
Kir2.1通道基因诱导功能障碍：对短QT3综合征和自闭症-癫痫表型的影响
期刊:Human Molecular Genetics
影响因子:3.1
doi:10.1093/hmg/ddu201
Elena Ambrosini,Federico Sicca,Maria S Brignone,Maria C D'Adamo,Carlo Napolitano,Ilenio Servettini,Francesca Moro,Yanfei Ruan,Luca Guglielmi,Stefania Pieroni,Giuseppe Servillo,Angela Lanciotti,Giulia Valvo,Luigi Catacuzzeno,Fabio Franciolini,Paola Molinari,Maria Marchese,Alessandro Grottesi,Renzo Guerrini,Filippo M Santorelli,Silvia Priori,Mauro Pessia
