Farrugia, A.; Rollet, K.; Sinniger, J.; Brun, S.; Spenle, C.; Ludes, B.; Taleb, O.; Mensah-Nyagan, A.G.
H1153Y-KCNH2 Mutation Identified in a Sudden Arrhythmic Death Syndrome Case Alters Channel Gating. Int. J. Mol. Sci. 2021, 22, 9235.
https://doi.org/10.3390/ijms22179235
AMA Style
Farrugia A, Rollet K, Sinniger J, Brun S, Spenle C, Ludes B, Taleb O, Mensah-Nyagan AG.
H1153Y-KCNH2 Mutation Identified in a Sudden Arrhythmic Death Syndrome Case Alters Channel Gating. International Journal of Molecular Sciences. 2021; 22(17):9235.
https://doi.org/10.3390/ijms22179235
Chicago/Turabian Style
Farrugia, Audrey, Kevin Rollet, Jérome Sinniger, Susana Brun, Caroline Spenle, Bertrand Ludes, Omar Taleb, and Ayikoe Guy Mensah-Nyagan.
2021. "H1153Y-KCNH2 Mutation Identified in a Sudden Arrhythmic Death Syndrome Case Alters Channel Gating" International Journal of Molecular Sciences 22, no. 17: 9235.
https://doi.org/10.3390/ijms22179235
APA Style
Farrugia, A., Rollet, K., Sinniger, J., Brun, S., Spenle, C., Ludes, B., Taleb, O., & Mensah-Nyagan, A. G.
(2021). H1153Y-KCNH2 Mutation Identified in a Sudden Arrhythmic Death Syndrome Case Alters Channel Gating. International Journal of Molecular Sciences, 22(17), 9235.
https://doi.org/10.3390/ijms22179235