AB47-2: Mutations in the cardiac sodium channel, SCN5A, are a rare cause of familial atrial fibrillation

Autor: Ellinor, Patrick T., Nam, Edwin G., Shea, Marisa A., Ruskin, Jeremy N., Macrae, Calum A.
Zdroj: In Heart Rhythm 2006 3(5) Supplement:S97-S97
Databáze: ScienceDirect