Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls
Walsh, R, Lahrouchi, N, Tadros, R, Kyndt, F, Glinge, C, Postema, Pg, Amin, As, Nannenberg, Ea, Ware, Js, Whiffin, N, Mazzarotto, F, Škorić-Milosavljević, D, Krijger, C, Arbelo, E, Babuty, D, Barajas-Martinez, H, Beckmann, Bm, Bézieau, S, Bos, Jm, Breckpot, J, Campuzano, O, Castelletti, S, Celen, C, Clauss, S, Corveleyn, A, Crotti, L, Dagradi, F, de Asmundis, C, Denjoy, I, Dittmann, S, Ellinor, Pt, Ortuño, Cg, Giustetto, C, Gourraud, Jb, Hazeki, D, Horie, M, Ishikawa, T, Itoh, H, Kaneko, Y, Kanters, Jk, Kimoto, H, Kotta, Mc, Krapels, Ipc, Kurabayashi, M, Lazarte, J, Leenhardt, A, Loeys, Bl, Lundin, C, Makiyama, T, Mansourati, J, Martins, Rp, Mazzanti, A, Mörner, S, Napolitano, C, Ohkubo, K, Papadakis, M, Rudic, B, Molina, Ms, Sacher, F, Sahin, H, Sarquella-Brugada, G, Sebastiano, R, Sharma, S, Sheppard, Mn, Shimamoto, K, Shoemaker, Mb, Stallmeyer, B, Steinfurt, J, Tanaka, Y, Tester, Dj, Usuda, K, van der Zwaag, Pa, van Dooren, S, van Laer, L, Winbo, A, Winkel, Bg, Yamagata, K, Zumhagen, S, Volders, Pga, Lubitz, Sa, Antzelevitch, C, Platonov, Pg, Odening, Ke, Roden, Dm, Roberts, Jd, Skinner, Jr, Tfelt-Hansen, J, van den Berg, Mp, Olesen, Ms, Lambiase, Pd, Borggrefe, M, Hayashi, K, Rydberg, A, Nakajima, T, Yoshinaga, M, Saenen, Jb, Kääb, S, Brugada, P, Robyns, T, Giachino, Df
Published in Genetics in medicine (23.01.2021)
Published in Genetics in medicine (23.01.2021)
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