@misc{indiciae690d8f390e73,
  title = {Whole-genome sequencing implicates rare, low-frequency and structural non-coding variation at the SCN5A locus in Brugada syndrome.},
  author = {Alex Lipov and Manon Baudic and Pierre Lindenbaum and Isabella Mengarelli and Matthew J O'Neill and Fernanda M Bosada and Yanushi Wijeyeratne and Luis de la Higuera Romero and Maarten Kooyman and Marion Gaudin and Graziella Aquilina and Leander Beekman and Estelle Baron and Mathilde Bertrand and Zoya Kingsbury and Mark T Ross and Marre Corver and Paola Lombardi and Ingrid Krapels and Paul G Volders and Rafik Tadros and Fenna Tuijnenburg and Karel van Duijvenboden and Ammar Al-Chalabi and Jan H Veldink and Sean J Jurgens and Aur\&\#xe9;lie Thollet and Eric Charpentier and Camille Maiano and Philippe Mabo and Antoine Leenhardt and Frederic Sacher and Arjan C Houweling and Hanno L Tan and Vincent M Christoffels and Michael W Tanck and Andrew Grace and Koonlawee Nademanee and Apichai Khongphatthanayothin and Andrew M Glazer and Jean Fran\&\#xe7;ois Deleuze and FranceGenRef consortium and Juan Pablo Ochoa and J\&\#xe9;r\&\#xf4;me Montnach and Michel De Waard and Pieter G Postema and Ahmad S Amin and Jean-Baptiste Gourraud and Pascale Guicheney and Dan M Roden and Jean-Jacques Schott and Christian Dina and Vincent Probst and Pier D Lambiase and Elijah R Behr and Arthur A M Wilde and Richard Redon and Roddy Walsh and Julien Barc and Connie R Bezzina},
  year = {2026},
  doi = {10.64898/2026.07.07.26356386},
  url = {https://pubmed.ncbi.nlm.nih.gov/42465902/},
  note = {Source identifier: 42465902}
}