scholarly journals Uncoupling sodium channel dimers restores the phenotype of a pain‐linked Na v 1.7 channel mutation

2020 ◽  
Vol 177 (19) ◽  
pp. 4481-4496 ◽  
Author(s):  
Annika H. Rühlmann ◽  
Jannis Körner ◽  
Ralf Hausmann ◽  
Nikolay Bebrivenski ◽  
Christian Neuhof ◽  
...  
Keyword(s):  
Sodium Channel ◽  
Channel Mutation

scholarly journals A cardiac sodium channel mutation identified in Brugada syndrome associated with atrial standstill

2004 ◽  
Vol 255 (1) ◽  
pp. 137-142 ◽  
Author(s):  
N. Takehara ◽  
N. Makita ◽  
J. Kawabe ◽  
N. Sato ◽  
Y. Kawamura ◽  
...  
Keyword(s):  
Sodium Channel ◽  
Brugada Syndrome ◽  
Cardiac Sodium Channel ◽  
Channel Mutation ◽  
Sodium Channel Mutation

scholarly journals Characterization of a new sodium channel mutation at arginine 1448 associated with moderate paramyotonia congenita in humans

1999 ◽  
Vol 518 (2) ◽  
pp. 337-344 ◽  
Author(s):  
Saïd Bendahhou ◽  
Theodore R. Cummins ◽  
Hubert Kwiecinski ◽  
Stephen G. Waxman ◽  
Louis J. Ptácek
Keyword(s):  
Sodium Channel ◽  
Paramyotonia Congenita ◽  
Channel Mutation ◽  
Sodium Channel Mutation

Cardiac sodium channel mutation in atrial fibrillation

Heart Rhythm ◽  
2008 ◽  
Vol 5 (1) ◽  
pp. 99-105 ◽  
Author(s):  
Patrick T. Ellinor ◽  
Edwin G. Nam ◽  
Marisa A. Shea ◽  
David J. Milan ◽  
Jeremy N. Ruskin ◽  
...  
Keyword(s):  
Atrial Fibrillation ◽  
Sodium Channel ◽  
Cardiac Sodium Channel ◽  
Channel Mutation ◽  
Sodium Channel Mutation

A skeletal muscle sodium channel mutation in a Japanese family with paramyotonia congenita

1995 ◽  
Vol 133 (1-2) ◽  
pp. 192-193 ◽  
Author(s):  
Takeshi Yamada ◽  
Hirofumi Ochi ◽  
Hideo Hara ◽  
Takeo Yoshimura ◽  
Takuro Kobayashi
Keyword(s):  
Skeletal Muscle ◽  
Sodium Channel ◽  
Japanese Family ◽  
Paramyotonia Congenita ◽  
Channel Mutation ◽  
Sodium Channel Mutation
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