Two long QT syndrome loci map to chromosomes 3 and 7 with evidence for further heterogeneity

[1]  M. Keating,et al.  A new form of long QT syndrome associated with syndactyly. , 1995, Journal of the American College of Cardiology.

[2]  P. Schwartz,et al.  Evidence of Genetic Heterogeneity in Romano‐Ward Long QT syndrome: Analysis of 23 Families , 1994, Circulation.

[3]  M. Lehmann,et al.  T wave "humps" as a potential electrocardiographic marker of the long QT syndrome. , 1994, Journal of the American College of Cardiology.

[4]  Cécile Fizames,et al.  The 1993–94 Généthon human genetic linkage map , 1994, Nature Genetics.

[5]  H. Massa,et al.  Integration of physical, genetic and cytogenetic maps of human chromosome 7: isolation and analysis of yeast artificial chromosome clones for 117 mapped genetic markers. , 1994, Human molecular genetics.

[6]  J. Seidman,et al.  A complex bilateral polysyndactyly disease locus maps to chromosome 7q36 , 1994, Nature Genetics.

[7]  C. Lang,et al.  QT dispersion and sudden unexpected death in chronic heart failure , 1994, The Lancet.

[8]  Mark Keating Genetics of the Long QT Syndrome , 1994, Journal of cardiovascular electrophysiology.

[9]  Jean Weissenbach,et al.  The gene for triphalangeal thumb maps to the subtelomeric region of chromosome 7q , 1994, Nature Genetics.

[10]  R. Myerburg,et al.  Sudden Cardiac Death: Epidemiology, Transient Risk, and Intervention Assessment , 1993, Annals of Internal Medicine.

[11]  J. Kennedy,et al.  The D4 dopamine receptor gene maps on 11p proximal to HRAS. , 1993, Genomics.

[12]  J. Mason A comparison of seven antiarrhythmic drugs in patients with ventricular tachyarrhythmias. Electrophysiologic Study versus Electrocardiographic Monitoring Investigators. , 1993, The New England journal of medicine.

[13]  J. Mason A comparison of electrophysiologic testing with Holter monitoring to predict antiarrhythmic-drug efficacy for ventricular tachyarrhythmias. Electrophysiologic Study versus Electrocardiographic Monitoring Investigators. , 1993, The New England journal of medicine.

[14]  M. Leppert,et al.  Locus heterogeneity of autosomal dominant long QT syndrome. , 1993, The Journal of clinical investigation.

[15]  B. Kerem,et al.  Evidence of genetic heterogeneity in the long QT syndrome. , 1993, Science.

[16]  M. Crackower,et al.  Molecular basis of Thomsen's disease (autosomal dominant myotonia congenita) , 1993, Nature Genetics.

[17]  Assignment of human potassium channel gene KCNA4 (Kv1.4, PCN2) to chromosome 11q13.4-->q14.1. , 1993, Genomics.

[18]  B. Rudy,et al.  Localization of a highly conserved human potassium channel gene (NGK2-KV4; KCNC1) to chromosome 11p15. , 1993, Genomics.

[19]  G. Gyapay,et al.  A second-generation linkage map of the human genome , 1992, Nature.

[20]  M. Leppert,et al.  The spectrum of symptoms and QT intervals in carriers of the gene for the long-QT syndrome. , 1992, The New England journal of medicine.

[21]  K. Grzeschik,et al.  The skeletal muscle chloride channel in dominant and recessive human myotonia. , 1992, Science.

[22]  R. Espinosa,et al.  Assignment of the gene encoding the alpha 1 subunit of the neuroendocrine/brain-type calcium channel (CACNL1A2) to human chromosome 3, band p14.3. , 1992, Genomics.

[23]  Mark Keating Linkage Analysis and Long QT Syndrome: Using Genetics to Study Cardiovascular Disease , 1992, Circulation.

[24]  Mark E. Williams,et al.  Structure and functional expression of α 1, α 2, and β subunits of a novel human neuronal calcium channel subtype , 1992, Neuron.

[25]  G. Bell,et al.  Cloning of the alpha 1 subunit of a voltage-dependent calcium channel expressed in pancreatic beta cells. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[26]  M. Leppert,et al.  Consistent linkage of the long-QT syndrome to the Harvey ras-1 locus on chromosome 11. , 1991, American journal of human genetics.

[27]  C. Kozak,et al.  A brain L-type calcium channel alpha 1 subunit gene (CCHL1A2) maps to mouse chromosome 14 and human chromosome 3. , 1991, Genomics.

[28]  M. Leppert,et al.  Linkage of a cardiac arrhythmia, the long QT syndrome, and the Harvey ras-1 gene. , 1991, Science.

[29]  D. Albertson,et al.  The use of double colour plasmid fluorescence in situ hybridisation to order markers for nine polymorphic loci on 3p , 1991 .

[30]  Brien,et al.  Abstracts for the committee on the genetic constitution of chromosome 1 , 1991 .

[31]  A. Brown,et al.  ras p21 and GAP inhibit coupling of muscarinic receptors to atrial K+ channels , 1990, Cell.

[32]  J. Mccomb,et al.  QT dispersion: an indication of arrhythmia risk in patients with long QT intervals. , 1990, British heart journal.

[33]  R. Goyal Muscarinic receptor subtypes. Physiology and clinical implications. , 1989, The New England journal of medicine.

[34]  Craig T. January,et al.  Early Afterdepolarizations: Mechanism of Induction and Block A Role for L‐Type Ca2+ Current , 1989, Circulation research.

[35]  J. Weber,et al.  Abundant class of human DNA polymorphisms which can be typed using the polymerase chain reaction. , 1989, American journal of human genetics.

[36]  C. Antzelevitch,et al.  Quinidine-induced action potential prolongation, early afterdepolarizations, and triggered activity in canine Purkinje fibers. Effects of stimulation rate, potassium, and magnesium. , 1989, Circulation.

[37]  C. January,et al.  A Model for Early Afterdepolarizations: Induction With the Ca2+ Channel Agonist Bay K 8644 , 1988, Circulation research.

[38]  D. Levy,et al.  Circadian variation in the incidence of sudden cardiac death in the Framingham Heart Study population. , 1987, The American journal of cardiology.

[39]  T. Bonner,et al.  Identification of a family of muscarinic acetylcholine receptor genes. , 1987, Science.

[40]  D. Zipes Proarrhythmic effects of antiarrhythmic drugs. , 1987, The American journal of cardiology.

[41]  R. D'Agostino,et al.  Sudden death risk in overt coronary heart disease: the Framingham Study. , 1987, American heart journal.

[42]  N E Morton,et al.  Report of the Committee on Methods of Linkage Analysis and Reporting. , 1985, Cytogenetics and cell genetics.

[43]  J. Ott,et al.  Multilocus linkage analysis in humans: detection of linkage and estimation of recombination. , 1985, American journal of human genetics.

[44]  J. Ott,et al.  Linkage analysis and family classification under heterogeneity , 1983, Annals of human genetics.

[45]  P. Penkoske,et al.  Disparate Electrophysiological Alterations Accompanying Dysrhythmia due to Coronary Occlusion and Reperfusion in the Cat , 1978, Circulation.

[46]  P. Schwartz,et al.  QT interval prolongation as predictor of sudden death in patients with myocardial infarction. , 1978, Circulation.

[47]  D. Durrer,et al.  The Effect of Acute Coronary Artery Occlusion on Subepicardial Transmembrane Potentials in the Intact Porcine Heart , 1977, Circulation.

[48]  A. Malliani,et al.  The long Q-T syndrome. , 1975, American heart journal.

[49]  J. .. Abildskov,et al.  Q-T interval syndromes. , 1974, Progress in cardiovascular diseases.

[50]  Ward Oc A NEW FAMILIAL CARDIAC SYNDROME IN CHILDREN. , 1964 .

[51]  C. Brooks,et al.  Excitability and electrical response of ischemic heart muscle. , 1960, The American journal of physiology.

[52]  A. Jervell,et al.  Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval, and sudden death , 1957 .