基因编辑仓鼠Trafficking-deficient long QT syndrome mutation KCNQ1-T587M confers severe clinical phenotype by impairment of KCNH2 membrane localization: evidence for clinically significant IKr-IKs alpha-subunit interaction.
期刊:Heart rhythm发表年份:2009作者:Peter Biliczki; Zenawit Girmatsion; Ralf P Brandes; Sabine Harenkamp; Bruno Pitard; Flavien Charpentier; Terence E Hébert; Stefan H Hohnloser; Isabelle Baró; Stanley Nattel; Joachim R Ehrlich
