Molecular diagnosis of the inherited long-QT syndrome in a woman who died after near-drowning

被引：96

作者：

Ackerman, MJ

Tester, DJ

Porter, CJ

Edwards, WD

机构：

[1] Mayo Clin & Mayo Fdn, Dept Pediat & Adolescent Med, Mayo Eugenio Litta Childrens Hosp, Pediat Cardiol Sect, Rochester, MN 55905 USA

[2] Mayo Clin & Mayo Fdn, Dept Lab Med & Pathol, Rochester, MN 55905 USA

来源：

NEW ENGLAND JOURNAL OF MEDICINE | 1999年 / 341卷 / 15期

关键词：

D O I：

10.1056/NEJM199910073411504

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

[No abstract available]

引用

页码：1121 / 1125

页数：5

共 14 条

[1] MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia
Abbott, GW
Sesti, F
Splawski, I
Buck, ME
Lehmann, WH
Timothy, KW
Keating, MT
Goldstein, SAN
[J]. CELL, 1999, 97 (02) : 175 - 187
[2] A novel mutation in KVLQT1 is the molecular basis of inherited long QT syndrome in a near-drowning patient's family
Ackerman, MJ
Schroeder, JJ
Berry, R
Schaid, DJ
Porter, CBJ
Michels, VV
Thibodeau, SN
[J]. PEDIATRIC RESEARCH, 1998, 44 (02) : 148 - 153
[3] The long QT syndrome: Ion channel diseases of the heart
Ackerman, MJ
[J]. MAYO CLINIC PROCEEDINGS, 1998, 73 (03) : 250 - 269
[4] ANDERSON MA, 1984, IN VITRO CELL DEV B, V20, P856
[5] THE LONG QT SYNDROME IN CHILDREN - AN INTERNATIONAL STUDY OF 287 PATIENTS
GARSON, A
DICK, M
FOURNIER, A
GILLETTE, PC
HAMILTON, R
KUGLER, JD
VANHARE, GF
VETTER, V
VICK, GW
[J]. CIRCULATION, 1993, 87 (06) : 1866 - 1872
[6] Kallas Harry J., 1993, Current Opinion in Pediatrics, V5, P295
[7] Impact of laboratory molecular diagnosis on contemporary diagnostic criteria for genetically transmitted cardiovascular diseases: Hypertrophic cardiomyopathy, long-QT syndrome, and Marfan syndrome - A statement for healthcare professionals from the councils on clinical cardiology, cardiovascular disease in the young, and basic science, American Heart Association
Maron, BJ
Moller, JH
Seidman, CE
Vincent, GM
Dietz, HC
Moss, AJ
Towbin, JA
Sondheimer, HM
Pyeritz, RE
McGee, G
Epstein, AE
[J]. CIRCULATION, 1998, 98 (14) : 1460 - 1471
[8] Mizuta Ryuzo, 1993, Acta Paediatrica Japonica, V35, P186
[9] THE LONG QT SYNDROME - PROSPECTIVE LONGITUDINAL-STUDY OF 328 FAMILIES
MOSS, AJ
SCHWARTZ, PJ
CRAMPTON, RS
TZIVONI, D
LOCATI, EH
MACCLUER, J
HALL, WJ
WEITKAMP, L
VINCENT, GM
GARSON, A
ROBINSON, JL
BENHORIN, J
CHOI, SS
[J]. CIRCULATION, 1991, 84 (03) : 1136 - 1144
[10] ECG T-WAVE PATTERNS IN GENETICALLY DISTINCT FORMS OF THE HEREDITARY LONG QT SYNDROME
MOSS, AJ
ZAREBA, W
BENHORIN, J
LOCATI, EH
HALL, WJ
ROBINSON, JL
SCHWARTZ, PJ
TOWBIN, JA
VINCENT, GM
LEHMANN, MH
KEATING, MT
MACCLUER, JW
TIMOTHY, KW
[J]. CIRCULATION, 1995, 92 (10) : 2929 - 2934

← 1 2 →