Yamamura K et al. (2010). A novel SCN5A mutation associated with the linker between III and IV domains of Nav1.5 in a neonate with fatal long QT syndrome. International journal of cardiology. 145 [PubMed]

See more from authors: Yamamura K · Muneuchi J · Uike K · Ikeda K · Inoue H · Takahata Y · Shiokawa Y · Yoshikane Y · Makiyama T · Horie M · Hara T

References and models cited by this paper
References and models that cite this paper

Song W et al. (2012). The human Nav1.5 F1486 deletion associated with long QT syndrome leads to impaired sodium channel inactivation and reduced lidocaine sensitivity. The Journal of physiology. 590 [PubMed]

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