| 1 | BRGS1, BRGS10, BRGS2, BRGS3, BRGS4, BRGS5, BRGS6, BRGS7, BRGS9, CACN2B, CACNA1C, GPD1L, KCNE3, SCN1B, SCN3B, SCN5A
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| The genetic basis of Brugada syndrome: a mutation update.
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| Hedley PL, Jørgensen P, Schlamowitz S, Moolman-Smook J, Kanters JK, Corfield VA, Christiansen M.
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| Hum Mutat 30(9):1256-66. Review.PMID: 19606473 2009
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| 2 | BRGS4, CACNB2
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| Accelerated inactivation of the L-type calcium current due to a mutation in CACNB2b underlies Brugada syndrome.
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| Cordeiro JM, Marieb M, Pfeiffer R, Calloe K, Burashnikov E, Antzelevitch C.
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| J Mol Cell Cardiol 46(5):695-703.
2009
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| 3 | BRGS1, BRGS10, BRGS3, BRGS4
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| Clinical aspects and prognosis of Brugada syndrome in children.
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| Probst V, Denjoy I, Meregalli PG, Amirault JC, Sacher F, Mansourati J, Babuty D, Villain E, Victor J, Schott JJ, Lupoglazoff JM, Mabo P, Veltmann C, Jesel L, Chevalier P, Clur SA, Haissaguerre M, Wolpert C, Le Marec H, Wilde AA.
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| Circulation 115(15):2042-8. Epub 2007 Apr 2. 2007
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