Prevalence and Spectrum of Large Deletions or Duplications in the Major Long QT Syndrome-Susceptibility Genes and Implications for Long QT Syndrome Genetic Testing-Reference-Cited by-同舟云学术

Prevalence and Spectrum of Large Deletions or Duplications in the Major Long QT Syndrome-Susceptibility Genes and Implications for Long QT Syndrome Genetic Testing

Published:2010-10 Issue:8 Volume:106 Page:1124-1128
ISSN:0002-9149
Container-title:The American Journal of Cardiology
language:en
Short-container-title:The American Journal of Cardiology

Author:

Tester David J.,Benton Amber J.,Train Laura,Deal Barbara,Baudhuin Linnea M.,Ackerman Michael J.

Funder

Mayo Clinic

National Institutes of Health

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference19 articles.

1. Long QT syndrome caused by a large duplication in the KCNH2 (HERG) gene undetectable by current polymerase chain reaction-based exon-scanning methodologies;Koopmann;Heart Rhythm,2006

2. Identification of large gene deletions and duplications in KCNQ1 and KCNH2 in patients with long QT syndrome [see comment];Eddy;Heart Rhythm,2008

3. Delineation of the phenotype associated with 7q36.1q36.2 deletion: long QT syndrome, renal hypoplasia and mental retardation;Caselli;Am J Med Genet A,2008

4. Diagnostic criteria for the long QT syndrome;Schwartz;Circulation,1993

5. Genomic structure of three long QT syndrome genes: KVLQT1, HERG, and KCNE1;Splawski;Genomics,1998

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