APA
Behr E. R., Savio-Galimberti E., Barc J., Holst A. G., Petropoulou E., Prins B. P., Jabbari J., Torchio M., Berthet M., Mizusawa Y., Yang T., Nannenberg E. A., Dagradi F., Weeke P., Bastiaenan R., Ackerman M. J., Haunso S., Leenhardt A., Kääb S., Probst V., Redon R., Sharma S., Wilde A., Tfelt-Hansen J., Schwartz P., Roden D. M., Bezzina C. R., Olesen M., Darbar D., Guicheney P., Crotti L. & Jamshidi Y. (20160210). Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study. : Cardiovascular research.
Chicago
Behr Elijah R, Savio-Galimberti Eleonora, Barc Julien, Holst Anders G, Petropoulou Evmorfia, Prins Bram P, Jabbari Javad, Torchio Margherita, Berthet Myriam, Mizusawa Yuka, Yang Tao, Nannenberg Eline A, Dagradi Federica, Weeke Peter, Bastiaenan Rachel, Ackerman Michael J, Haunso Stig, Leenhardt Antoine, Kääb Stefan, Probst Vincent, Redon Richard, Sharma Sanjay, Wilde Arthur, Tfelt-Hansen Jacob, Schwartz Peter, Roden Dan M, Bezzina Connie R, Olesen Morten, Darbar Dawood, Guicheney Pascale, Crotti Lia and Jamshidi Yalda. 20160210. Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study. : Cardiovascular research.
Harvard
Behr E. R., Savio-Galimberti E., Barc J., Holst A. G., Petropoulou E., Prins B. P., Jabbari J., Torchio M., Berthet M., Mizusawa Y., Yang T., Nannenberg E. A., Dagradi F., Weeke P., Bastiaenan R., Ackerman M. J., Haunso S., Leenhardt A., Kääb S., Probst V., Redon R., Sharma S., Wilde A., Tfelt-Hansen J., Schwartz P., Roden D. M., Bezzina C. R., Olesen M., Darbar D., Guicheney P., Crotti L. and Jamshidi Y. (20160210). Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study. : Cardiovascular research.
MLA
Behr Elijah R, Savio-Galimberti Eleonora, Barc Julien, Holst Anders G, Petropoulou Evmorfia, Prins Bram P, Jabbari Javad, Torchio Margherita, Berthet Myriam, Mizusawa Yuka, Yang Tao, Nannenberg Eline A, Dagradi Federica, Weeke Peter, Bastiaenan Rachel, Ackerman Michael J, Haunso Stig, Leenhardt Antoine, Kääb Stefan, Probst Vincent, Redon Richard, Sharma Sanjay, Wilde Arthur, Tfelt-Hansen Jacob, Schwartz Peter, Roden Dan M, Bezzina Connie R, Olesen Morten, Darbar Dawood, Guicheney Pascale, Crotti Lia and Jamshidi Yalda. Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study. : Cardiovascular research. 20160210.