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2. [Detection of gene mutations of SCN5A in 7 patients with Brugada syndrome]. Yuan BB; Shan QJ; Yang B; Chen ML; Zou JG; Chen C; Xu DJ; Cao KJ Zhonghua Xin Xue Guan Bing Za Zhi; 2008 May; 36(5):404-7. PubMed ID: 19100032 [TBL] [Abstract][Full Text] [Related]
3. [Novel SCN5A gene mutations associated with Brugada syndrome: V95I, A1649V and delF1617]. Liang P; Liu WL; Hu DY; Li CL; Tao WH; Li L Zhonghua Xin Xue Guan Bing Za Zhi; 2006 Jul; 34(7):616-9. PubMed ID: 17081365 [TBL] [Abstract][Full Text] [Related]
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10. Structural myocardial abnormalities in asymptomatic family members with Brugada syndrome and SCN5A gene mutation. Frustaci A; Russo MA; Chimenti C Eur Heart J; 2009 Jul; 30(14):1763. PubMed ID: 19411664 [No Abstract] [Full Text] [Related]
11. The occurrence of Brugada syndrome and isolated cardiac conductive disease in the same family could be due to a single SCN5A mutation or to the accidental association of both diseases. Six I; Hermida JS; Huang H; Gouas L; Fressart V; Benammar N; Hainque B; Denjoy I; Chahine M; Guicheney P Europace; 2008 Jan; 10(1):79-85. PubMed ID: 18156160 [TBL] [Abstract][Full Text] [Related]
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