ModelDB: Paper information

Ruan Y et al. (2010). Trafficking defects and gating abnormalities of a novel SCN5A mutation question gene-specific therapy in long QT syndrome type 3. Circulation research. 106 [PubMed]

See more from authors: Ruan Y · Denegri M · Liu N · Bachetti T · Seregni M · Morotti S · Severi S · Napolitano C · Priori SG

References and models cited by this paper

References and models that cite this paper

Gurkiewicz M, Korngreen A, Waxman SG, Lampert A. (2011). Kinetic modeling of Nav1.7 provides insight into erythromelalgia-associated F1449V mutation. Journal of neurophysiology. 105 [PubMed]

HMM of Nav1.7 WT and F1449V (Gurkiewicz et al. 2011) [Model]

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]