| 1 | PCCD1, SCN5A
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| Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenegre disease.
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| Probst V, Kyndt F, Potet F, Trochu JN, Mialet G, Demolombe S, Schott JJ, Baro I, Escande D, Le Marec H.
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| J Am Coll Cardiol 41(4):643-52. 2003
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| 2 | PCCD1, SCN5A
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| A sodium-channel mutation causes isolated cardiac conduction disease.
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| tan Hl, Bink-Boelkens MTE, Bezzina CR, Viswanathan PC, Beaufort-Krol GCM, van Tintelen PJ, van den Berg MP, Wilde AAM, Baiser JR.
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| Nature 409 : 1043. 2001
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| 3 | PCCD1, PCCD2, SCN5A
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| A novel SCN5A mutation associated with idiopathic ventricular fibrillation without typical ECG findings of Brugada syndrome.
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| Akai J, Makita N, Sakurada H, Shirai N, Ueda K, Kitabatake A, Nakazawa K, Kimura A, Hiraoka M.
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| FEBS Lett 479(1-2):29-34. 2000
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| 4 | PCCD1, SCN5A
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| Cardiac conduction defects associate with mutations in SCN5A.
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| Schott JJ, et al.
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| Nat Genet 23(1):20-1. No abstract available 1999
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