RYR2 and CASQ2 mutations in patients suffering from catecholaminergic polymorphic ventricular tachycardia

被引:37
作者
Lahat, H [1 ]
Pras, E
Eldar, M
机构
[1] Tel Aviv Univ, Chaim Sheba Med Ctr, Genet Inst, Tel Hashomer, Israel
[2] Tel Aviv Univ, Chaim Sheba Med Ctr, Inst Heart, Tel Hashomer, Israel
关键词
D O I
10.1161/01.CIR.0000050555.40735.ED
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
收藏
页码:E29 / E29
页数:1
相关论文
共 5 条
  • [1] A missense mutation in a highly conserved region of CASQ2 is associated with autosomal recessive catecholamine-induced polymorphic ventricular tachycardia in Bedouin families from Israel
    Lahat, H
    Pras, E
    Olender, T
    Avidan, N
    Ben-Asher, E
    Man, O
    Levy-Nissenbaum, E
    Khoury, A
    Lorber, A
    Goldman, B
    Lancet, D
    Eldar, M
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (06) : 1378 - 1384
  • [2] Lahat H, 2001, CIRCULATION, V103, P2822
  • [3] Clinical and molecular characterization of patients with catecholaminergic polymorphic ventricular tachycardia
    Priori, SG
    Napolitano, C
    Memmi, M
    Colombi, B
    Drago, F
    Gasparini, M
    DeSimone, L
    Coltorti, F
    Bloise, R
    Keegan, R
    Cruz, FES
    Vignati, G
    Benatar, A
    DeLogu, A
    [J]. CIRCULATION, 2002, 106 (01) : 69 - 74
  • [4] Priori SG, 2001, CIRCULATION, V103, P196
  • [5] Arrhythmic disorder mapped to chromosome 1q42-q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts
    Swan, H
    Piippo, K
    Viitasalo, M
    Heikkilä, P
    Paavonen, T
    Kainulainen, K
    Kere, J
    Keto, P
    Kontula, K
    Toivonen, L
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1999, 34 (07) : 2035 - 2042