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Dive into the research topics of 'R231C mutation in KCNQ1 causes long QT syndrome type 1 and familial atrial fibrillation'. Together they form a unique fingerprint.- Sort by
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Daniel C. Bartos, Sabine Duchatelet, Don E. Burgess, Didier Klug, Isabelle Denjoy, Rachel Peat, Jean Marc Lupoglazoff, Vronique Fressart, Myriam Berthet, Michael J. Ackerman, Craig T. January, Pascale Guicheney, Brian P. Delisle
Research output: Contribution to journal › Article › peer-review