Associated Papers
Uncovering common genetic risk factors in migraine and epilepsy through whole exome sequencing.
Sahu P et al.
Epileptic Disorders : International Epilepsy Journal With Videotape, 2025
A Novel SCN5A Mutation (c.589G>A) Is Associated With Intermittent Atrial Standstill and Conduction System Disease.
Kohli U et al.
Jacc. Case Reports, 2025
Molecular interactions of the gating modifier toxin ProTx-II with NaV 1.5: implied existence of a novel toxin binding site coupled to activation.
Smith JJ et al.
The Journal of Biological Chemistry, 2007
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