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Volumn 11, Issue 6, 2000, Pages 710-712

Long QT syndrome: Ionic basis and arrhythmia mechanism long QT syndrome type 1

Author keywords

Delayed rectifier; Heart; KVLQT1; Potassium current

Indexed keywords

ALPHA CHAIN; AUTOSOMAL DOMINANT DISORDER; CHANNEL GATING; CHROMOSOME 11P; ELECTROCARDIOGRAM; GENE MAPPING; HEART VENTRICLE ARRHYTHMIA; HEART VENTRICLE FIBRILLATION; LONG QT SYNDROME; MISSENSE MUTATION; MOLECULAR CLONING; MUTATION; PERCEPTION DEAFNESS; POTASSIUM CURRENT; PRIORITY JOURNAL; RELIABILITY; REVIEW; SUDDEN DEATH; TORSADE DES POINTES;

EID: 0034047912     PISSN: 10453873     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1540-8167.2000.tb00035.x     Document Type: Review
Times cited : (42)

References (6)
  • 1
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    • Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene
    • 1. Keating M, Atkinson D, Dunn C, Timothy K. Vincent GM, Leppert M: Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene. Science 1991;252:704-706.
    • (1991) Science , vol.252 , pp. 704-706
    • Keating, M.1    Atkinson, D.2    Dunn, C.3    Timothy, K.4    Vincent, G.M.5    Leppert, M.6
  • 2
    • 9044240040 scopus 로고    scopus 로고
    • Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
    • 2. Wang Q, Curran ME, Splawski I, et al: Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias. Nat Genet 1996;12:17-23.
    • (1996) Nat Genet , vol.12 , pp. 17-23
    • Wang, Q.1    Curran, M.E.2    Splawski, I.3
  • 4
    • 0030799943 scopus 로고    scopus 로고
    • + channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias
    • + channel mutations in Romano-Ward and Jervell and Lange-Nielsen inherited cardiac arrhythmias. EMBO J 1997;16:5472-5479.
    • (1997) EMBO J , vol.16 , pp. 5472-5479
    • Chouabe, C.1    Neyroud, N.2    Guichney, P.3
  • 5
    • 0033065231 scopus 로고    scopus 로고
    • Functional effects of mutations in KvLQT1 that cause long QT syndrome
    • 5. Wang Z, Tristani-Firouzi M, Xu Q, et al: Functional effects of mutations in KvLQT1 that cause long QT syndrome. J Cardiovasc Electrophysiol 1999;10:817-826.
    • (1999) J Cardiovasc Electrophysiol , vol.10 , pp. 817-826
    • Wang, Z.1    Tristani-Firouzi, M.2    Xu, Q.3
  • 6
    • 0033597857 scopus 로고    scopus 로고
    • Long QT syndrome-associated mutations in the S4-S5 linker of KvLQT1 potassium channels modify gating and interaction with minK subunits
    • 6. Franqueza L, Lin M, Splawski I, et al: Long QT syndrome-associated mutations in the S4-S5 linker of KvLQT1 potassium channels modify gating and interaction with minK subunits. J Biol Chem 1999;274:21063-21070.
    • (1999) J Biol Chem , vol.274 , pp. 21063-21070
    • Franqueza, L.1    Lin, M.2    Splawski, I.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.