Circulation, Vol 85, 1973-1986, Copyright © 1992 by American Heart Association
M Keating
BACKGROUND. Recombinant DNA technologies have facilitated the development
of a set of polymorphic DNA markers covering the human genome. General
linkage analysis in families predisposed to inherited disease is now
feasible. Linkage analysis can help identify a disease gene even when
relatively little is known about the disorder. METHODS AND RESULTS. Using
this approach, we have identified linkage between a gene that causes the
long QT syndrome and DNA markers on chromosome 11. CONCLUSIONS. The
identification of the chromosomal location of the long QT locus is the
first step in defining the specific mutations that cause this disease.
ARTICLES
Linkage analysis and long QT syndrome. Using genetics to study cardiovascular disease
Department of Human Genetics, University of Utah Health Sciences Center, Salt Lake City.
This article has been cited by other articles:
![]() |
T. Nakajima, T. Furukawa, Y. Hirano, T. Tanaka, H. Sakurada, T. Takahashi, R. Nagai, T. Itoh, Y. Katayama, Y. Nakamura, et al. Voltage-shift of the current activation in HERG S4 mutation (R534C) in LQT2 Cardiovasc Res, November 1, 1999; 44(2): 283 - 293. [Abstract] [Full Text] [PDF] |
||||
![]() |
I. Splawski, K. W. Timothy, G. M. Vincent, D. L. Atkinson, and M. T. Keating Molecular Basis of the Long-QT Syndrome Associated with Deafness N. Engl. J. Med., May 29, 1997; 336(22): 1562 - 1567. [Full Text] [PDF] |
||||
![]() |
M. H. Lehmann, S. Hardy, D. Archibald, B. Quart, and D. J. MacNeil Sex Difference in Risk of Torsade de Pointes With d,l-Sotalol Circulation, November 15, 1996; 94(10): 2535 - 2541. [Abstract] [Full Text] |
||||
![]() |
M. T. Keating Genetic Approaches to Cardiovascular Disease : Supravalvular Aortic Stenosis, Williams Syndrome, and Long-QT syndrome Circulation, July 1, 1995; 92(1): 142 - 147. [Abstract] [Full Text] |
||||
![]() |
P. A. Brink, A. Ferreira, J. C. Moolman, H. W. Weymar, P.-L. van der Merwe, and V. A. Corfield Gene for Progressive Familial Heart Block Type I Maps to Chromosome 19q13 Circulation, March 15, 1995; 91(6): 1633 - 1640. [Abstract] [Full Text] |
||||
![]() |
R. R. Makkar, B. S. Fromm, R. T. Steinman, M. D. Meissner, and M. H. Lehmann Female Gender as a Risk Factor for Torsades de Pointes Associated With Cardiovascular Drugs JAMA, December 1, 1993; 270(21): 2590 - 2597. [Abstract] [PDF] |
||||
![]() |
M. Keating Response Science, June 25, 1993; 260(5116): 1962 - 1962. [PDF] |
||||
|
Circulation Home | Subscriptions | Archives | Feedback | Authors | Help | AHA Journals Home | Search Copyright © 1992 American Heart Association, Inc. All rights reserved. Unauthorized use prohibited. |