Editorial commentary: Will the real long QT genes please stand up
References (16)
A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
Cell
(1995)SCN5A mutations associated with an inherited cardiac arrhythmia, long QT syndrome
Cell
(1995)- et al.
Determining pathogenicity in cardiac genetic testing: filling in the blank spaces
Trends Cardiovasc Med
(2015) Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
Genet Med
(2015)Genetic purgatory and the cardiac channelopathies: Exposing the variants of uncertain/unknown significance issue
Heart Rhythm
(2015)Targeted mutational analysis of ankyrin-B in 541 consecutive, unrelated patients referred for long QT syndrome genetic testing and 200 healthy subjects
Heart Rhythm
(2005)Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen's Inherited Cardiomyopathy Expert Panel
Genet Med
(2018)Evaluating the clinical validity of gene-disease associations: an evidence-based framework developed by the clinical genome resource
Am J Hum Genet
(2017)
There are more references available in the full text version of this article.
Cited by (0)
View full text
© 2018 Elsevier Inc. All rights reserved.