Associated Papers
Predicting changes to INa from missense mutations in human SCN5A.
Clerx M et al.
Scientific Reports, 2018
30143662 (PubMed )
Supplement: 41598_2018_30577_MOESM1_ESM.pdf
Characterization of a novel Nav1.5 channel mutation, A551T, associated with Brugada syndrome.
Chiang KC et al.
Journal of Biomedical Science, 2009
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