Trafficking-deficient long QT syndrome mutation KCNQ1-T587M confers severe clinical phenotype by impairment of KCNH2 membrane localization: Evidence for clinically significant IKr-IKs α-subunit interaction
Titel:
Trafficking-deficient long QT syndrome mutation KCNQ1-T587M confers severe clinical phenotype by impairment of KCNH2 membrane localization: Evidence for clinically significant IKr-IKs α-subunit interaction
Auteur:
Biliczki, Peter Girmatsion, Zenawit Brandes, Ralf P. Harenkamp, Sabine Pitard, Bruno Charpentier, Flavien Hébert, Terence E. Hohnloser, Stefan H. Baró, Isabelle Nattel, Stanley Ehrlich, Joachim R.