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Whole-genome sequencing implicates rare, low-frequency and structural non-coding variation at the SCN5A locus in Brugada syndrome.

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Title: Whole-genome sequencing implicates rare, low-frequency and structural non-coding variation at the SCN5A locus in Brugada syndrome.
Authors: Lipov A, Baudic M, Lindenbaum P, Mengarelli I, O'Neill MJ, Bosada FM, Wijeyeratne Y, de la Higuera Romero L, Kooyman M, Gaudin M, Aquilina G, Beekman L, Baron E, Bertrand M, Kingsbury Z, Ross MT, Corver M, Lombardi P, Krapels I, Volders PG, Tadros R, Tuijnenburg F, van Duijvenboden K, Al-Chalabi A, Veldink JH, Jurgens SJ, Thollet A, Charpentier E, Maiano C, Mabo P, Leenhardt A, Sacher F, Houweling AC, Tan HL, Christoffels VM, Tanck MW, Grace A, Nademanee K, Khongphatthanayothin A, Glazer AM, Deleuze JF, Ochoa JP, Montnach J, De Waard M, Postema PG, Amin AS, Gourraud JB, Guicheney P, Roden DM, Schott JJ, Dina C, Probst V, Lambiase PD, Behr ER, Wilde AAM, Redon R, Walsh R, Barc J, Bezzina CR
Corporate Authors: FranceGenRef consortium
Source: MedRxiv : the preprint server for health sciences [medRxiv] 2026 Jul 10. Date of Electronic Publication: 2026 Jul 10.
Publication Type: Journal Article; Preprint
Journal Info: Country of Publication: United States NLM ID: 101767986 Publication Model: Electronic Cited Medium: Internet NLM ISO Abbreviation: medRxiv Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
FullText Text:
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DbLabel: MEDLINE Ultimate
An: 42465902
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PubType: Academic Journal
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        Value: 10.64898/2026.07.07.26356386
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        Text: English
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