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Volumn 85, Issue SUPPL. 1, 2002, Pages

Linkage analyses and SCN5A mutations screening in five Sudden Unexplained Death Syndrome (Lai-Tai) families

Author keywords

Autosomal Dominant; Brugada Syndrome; Lai Tai; SCN5A; Sudden Unexplained Death Syndrome

Indexed keywords

SODIUM CHANNEL; VOLTAGE GATED NA+ CHANNEL NA(V)1.5A; VOLTAGE-GATED NA+ CHANNEL NA(V)1.5A;

EID: 11244315277     PISSN: 01252208     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (15)

References (11)
  • 1
    • 0023282067 scopus 로고
    • Sudden unexplained death syndrome in Southeast Asian refugees: A review of CDC surveillance
    • Parrisk RG, Tucker M, Ing R, Encamacion C, Ebergardt M. Sudden unexplained death syndrome in Southeast Asian refugees: A review of CDC surveillance. MMWR CDC Surveil Summ 1987; 36:43SS-53SS.
    • (1987) MMWR CDC Surveil Summ , vol.36
    • Parrisk, R.G.1    Tucker, M.2    Ing, R.3    Encamacion, C.4    Ebergardt, M.5
  • 2
    • 0030850439 scopus 로고    scopus 로고
    • Arrhythmogenic marker for the sudden unexplained death syndrome in Thai men
    • Nademanee K, Veerakul G, Nimmannit S, et al. Arrhythmogenic marker for the sudden unexplained death syndrome in Thai men. Circulation 1997; 96: 2595-600.
    • (1997) Circulation , vol.96 , pp. 2595-2600
    • Nademanee, K.1    Veerakul, G.2    Nimmannit, S.3
  • 3
    • 0032546384 scopus 로고    scopus 로고
    • Genetic basis and molecular mechanism for idiopathic ventricular fibrillation
    • Chen Q, Kirsch GE, Zhang D, et al. Genetic basis and molecular mechanism for idiopathic ventricular fibrillation. Nature 1998; 392: 293-6.
    • (1998) Nature , vol.392 , pp. 293-296
    • Chen, Q.1    Kirsch, G.E.2    Zhang, D.3
  • 5
    • 0035380185 scopus 로고    scopus 로고
    • Pattern of inheritance in three sudden unexplained death syndrome ("Lai-Tai") families
    • Sangwatanaroj S, Ngamchareon C, Prechawat S. Pattern of inheritance in three sudden unexplained death syndrome ("Lai-Tai") families. J Med Assoc Thai 2001; 84 (Suppl 1): S443-S451.
    • (2001) J Med Assoc Thai , vol.84 , Issue.1 SUPPL.
    • Sangwatanaroj, S.1    Ngamchareon, C.2    Prechawat, S.3
  • 6
    • 18744429143 scopus 로고
    • The gene responsible for familial hypocalcemia map to chromsosome 3q in four unrelated families
    • Chou YHW, Brown EM, Levi T, et al. The gene responsible for familial hypocalcemia map to chromsosome 3q in four unrelated families. Nat Genet 1992; 1: 295-300.
    • (1992) Nat Genet , vol.1 , pp. 295-300
    • Chou, Y.H.W.1    Brown, E.M.2    Levi, T.3
  • 7
    • 0029992905 scopus 로고    scopus 로고
    • Genomic organization of the human SCN5A gene encoding the cardiac sodium channel
    • Wang Q, Li Z, Shen J, Keating MT. Genomic organization of the human SCN5A gene encoding the cardiac sodium channel. Genomics 1996; 34: 9-16.
    • (1996) Genomics , vol.34 , pp. 9-16
    • Wang, Q.1    Li, Z.2    Shen, J.3    Keating, M.T.4
  • 8
    • 1842267323 scopus 로고
    • Identification of mutations leading to the Lesch-Nyhan syndrome by automated direct sequencing of in vitro amplified cDNA
    • Gibbs RA, Nguyen PN, McBride LJ, Koepf SM, Caskey CT. Identification of mutations leading to the Lesch-Nyhan syndrome by automated direct sequencing of in vitro amplified cDNA. Proc Natl Acad Sci USA 1989; 86: 1919-23.
    • (1989) Proc Natl Acad Sci USA , vol.86 , pp. 1919-1923
    • Gibbs, R.A.1    Nguyen, P.N.2    McBride, L.J.3    Koepf, S.M.4    Caskey, C.T.5
  • 10
    • 11244260979 scopus 로고    scopus 로고
    • Genetics of sudden unexplained death: Pattern of inheritance in twenty-six "lai-tai" families
    • Sangwatanaroj S, Ngamcharoen C, Prechawat S, et al. Genetics of sudden unexplained death: Pattern of inheritance in twenty-six "lai-tai" families. Intern Med J Thai 2001; 17(Suppl): 74.
    • (2001) Intern Med J Thai , vol.17 , Issue.SUPPL. , pp. 74
    • Sangwatanaroj, S.1    Ngamcharoen, C.2    Prechawat, S.3
  • 11
    • 0034649298 scopus 로고    scopus 로고
    • Clinical and genetic eterogeneity of right bundle branch block and ST-segment elevation syndrome. A prospective evaluation of 52 families
    • Priori SG, Napolitano C, Gasparini M, et al. Clinical and genetic eterogeneity of right bundle branch block and ST-segment elevation syndrome. A prospective evaluation of 52 families. Circulation 2000; 102: 2509-15.
    • (2000) Circulation , vol.102 , pp. 2509-2515
    • Priori, S.G.1    Napolitano, C.2    Gasparini, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.