Whole-Genome Sequencing Can Identify Clinically Relevant Variants from a Single Sub-Punch of a Dried Blood Spot Specimen von McBride, David J, Fielding, Claire, Newington, Taksina, Vatsiou, Alexandra, Fischl, Harry, Bajracharya, Maya, Thomson, Vicki S, Fraser, Louise J, Fujita, Pauline A, Becq, Jennifer, Kingsbury, Zoya, Ross, Mark T, Moat, Stuart J, Morgan, Sian

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A Rare Noncoding Enhancer Variant in SCN5A Contributes to the High Prevalence of Brugada Syndrome in Thailand von Walsh, Roddy, Mauleekoonphairoj, John, Mengarelli, Isabella, Bosada, Fernanda M, Verkerk, Arie O, van Duijvenboden, Karel, Poovorawan, Yong, Wongcharoen, Wanwarang, Sutjaporn, Boosamas, Wandee, Pharawee, Chimparlee, Nitinan, Chokesuwattanaskul, Ronpichai, Vongpaisarnsin, Kornkiat, Dangkao, Piyawan, Wu, Cheng-I, Tadros, Rafik, Amin, Ahmad S, Lieve, Krystien V V, Postema, Pieter G, Kooyman, Maarten, Beekman, Leander, Sahasatas, Dujdao, Amnueypol, Montawatt, Krittayaphong, Rungroj, Prechawat, Somchai, Anannab, Alisara, Makarawate, Pattarapong, Ngarmukos, Tachapong, Phusanti, Keerapa, Veerakul, Gumpanart, Kingsbury, Zoya, Newington, Taksina, Maheswari, Uma, Ross, Mark T, Grace, Andrew, Lambiase, Pier D, Behr, Elijah R, Schott, Jean-Jacques, Redon, Richard, Barc, Julien, Christoffels, Vincent M, Wilde, Arthur A M, Nademanee, Koonlawee, Bezzina, Connie R, Khongphatthanayothin, Apichai

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