Skip to main navigation Skip to search Skip to main content

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

  • Elijah R. Behr
  • , Eleonora Savio-Galimberti
  • , Julien Barc
  • , Anders G. Holst
  • , Evmorfia Petropoulou
  • , Bram P. Prins
  • , Javad Jabbari
  • , Margherita Torchio
  • , Myriam Berthet
  • , Yuka Mizusawa
  • , Tao Yang
  • , Eline A. Nannenberg
  • , Federica Dagradi
  • , Peter Weeke
  • , Rachel Bastiaenan
  • , Michael J. Ackerman
  • , Stig Haunso
  • , Antoine Leenhardt
  • , Stefan Kääb
  • , Vincent Probst
  • Richard Redon, Sanjay Sharma, Arthur Wilde, Jacob Tfelt-Hansen, Peter Schwartz, Dan M. Roden, Connie R. Bezzina, Morten Olesen, Dawood Darbar, Pascale Guicheney, Lia Crotti, Yalda Jamshidi

Research output: Contribution to journalArticlepeer-review

Fingerprint

Dive into the research topics of 'Role of common and rare variants in SCN10A: Results from the Brugada syndrome QRS locus gene discovery collaborative study'. Together they form a unique fingerprint.
Sort by

Keyphrases

Biochemistry, Genetics and Molecular Biology