Genetically induced dysfunctions of Kir2.1 channels: implications for short QT3 syndrome and autism–epilepsy phenotype-Reference-Cited by-同舟云学术

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

Published:2014-05-02 Issue:18 Volume:23 Page:4875-4886
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:

Author:

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

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

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