Publication | Open Access
Mechanistic Basis for Type 2 Long QT Syndrome Caused by KCNH2 Mutations that Disrupt Conserved Arginine Residues in the Voltage Sensor
21
Citations
38
References
2013
Year
GeneticsMechanistic BasisType 2Molecular BiologyIon ChannelsElectrophysiologyKcnh2 MutationsMedicinePotassium Homeostasis
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