Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study

MLA

Peter Weeke, et al. Role of Common and Rare Variants in SCN10A: Results from the Brugada Syndrome QRS Locus Gene Discovery Collaborative Study. Jan. 2015. EBSCOhost, https://doi.org/10.1093/cvr/cvv042⟩.

APA

Peter Weeke, Bram P. Prins, Yalda Jamshidi, Stefan Kääb, Margherita Torchio, Evmorfia Petropoulou, Dan M. Roden, Sanjay Sharma, Eline A. Nannenberg, Lia Crotti, Pascale Guicheney, Javad Jabbari, Julien Barc, Tao Yang, Peter J. Schwartz, Anders G. Holst, Eleonora Savio-Galimberti, Morten S. Olesen, Michael J. Ackerman, … Jacob Tfelt-Hansen. (2015). Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study. https://doi.org/10.1093/cvr/cvv042⟩

Chicago

Peter Weeke, Bram P. Prins, Yalda Jamshidi, Stefan Kääb, Margherita Torchio, Evmorfia Petropoulou, Dan M. Roden, et al. 2015. “Role of Common and Rare Variants in SCN10A: Results from the Brugada Syndrome QRS Locus Gene Discovery Collaborative Study,” January. doi:10.1093/cvr/cvv042⟩.