Comparison of β1 and β3 subunit effects on long QT syndrome SCN5A mutations

被引:0
|
作者
Wang, DW
Makita, N
George, AL
机构
[1] Vanderbilt Univ, Med Ctr, Div Med Genet, Nashville, TN USA
[2] Hokkaido Univ, Dept Cardiovasc Med, Sapporo, Hokkaido, Japan
[3] Vanderbilt Univ, Med Ctr, Dept Pharmacol, Nashville, TN 37232 USA
关键词
D O I
暂无
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
引用
收藏
页码:423A / 423A
页数:1
相关论文
共 50 条
  • [21] Sodium channel abnormalities are infrequent in patients with long QT syndrome:: Identification of two novel SCN5A mutations
    Wattanasirichaigoon, D
    Vesely, MR
    Duggal, P
    Levine, JC
    Blume, ED
    Wolff, GS
    Edwards, SB
    Beggs, AH
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1999, 86 (05): : 470 - 476
  • [23] Cellular dysfunction of mutant SCN5A proteins causing long QT syndrome and Brugada syndrome
    You, S
    Wu, L
    Chen, S
    Wang, Q
    AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 71 (04) : 329 - 329
  • [24] Homozygote SCN5A mutation in long QT-syndrome with functional 2:1 AV block
    Denjoy, I
    Lupoglazoff, JM
    Cheav, T
    Baroudi, G
    Berthet, M
    Chahine, M
    Guicheney, P
    EUROPEAN HEART JOURNAL, 2001, 22 : 424 - 424
  • [25] A de novo missense mutation of the SCN5A gene in long QT syndrome.
    Matsuoka, R
    Yamagishi, H
    Furutani, M
    Kamisago, M
    Morikawa, Y
    Kojima, Y
    Hino, Y
    Furutani, Y
    Kimura, M
    Imamura, S
    Takao, A
    CIRCULATION, 1997, 96 (08) : 304 - 304
  • [26] NOVEL SCN5A MUTATION ASSOCIATED WITH LETHAL DRUG RESISTANT LONG QT SYNDROME
    Pournamdari, Ashley
    Wang, Jessica
    Nguyen, Thao P.
    George, Alfred
    Potet, Franck
    JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2022, 79 (09) : 2521 - 2521
  • [27] Developmental aspects of long QT syndrome type 3 and Brugada syndrome on the basis of a single SCN5A mutation in childhood
    Beaufort-Krol, GCM
    van den Berg, MP
    Wilde, AAM
    van Tintelen, JP
    Viersma, JW
    Bezzina, CR
    Bink-Boelkens, MTE
    JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2005, 46 (02) : 331 - 337
  • [28] Phenotype heterogeneity of SCN5A mutations in Brugada syndrome
    Ribouleau, G.
    Gourraud, J. B.
    Behar, N.
    Mansourati, J.
    Pierre, B.
    Cotard, V
    Thollet, A.
    Sacher, F.
    Wiart, F.
    Probst, V
    EUROPEAN HEART JOURNAL, 2024, 45
  • [29] Spectrum of mutations in long-QT syndrome genes KVLQT1, HERG, SCN5A, KCNE1, and KCNE2
    Splawski, I
    Shen, JX
    Timothy, KW
    Lehmann, MH
    Priori, S
    Robinson, JL
    Moss, AJ
    Schwartz, PJ
    Towbin, JA
    Vincent, GM
    Keating, MT
    CIRCULATION, 2000, 102 (10) : 1178 - 1185
  • [30] Mutations in the SCN5A promoter associated with Brugada syndrome
    Yagihara, N.
    Watanabe, H.
    Chatel, S.
    Barnett, P.
    Shimizu, W.
    Horie, M.
    Schott, J.
    Bezzina, C.
    Minamino, T.
    Makita, N.
    EUROPEAN HEART JOURNAL, 2013, 34 : 667 - 667