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Paper Details

Molecular diagnosis of long QT syndrome at 10 days of life by rapid whole genome sequencing.
Heart Rhythm
36
2014
KCNH2, LQTS, atrioventricular block, gene panel, human, human genes, infant, long QT syndrome, novel gene, rare disease, ventricular arrhythmias
Author NameAffiliation
James R PriestStanford University School of Medicine, Stanford University, California Child Health Research Institute Stanford Cardiovascular Institute
Frederick E DeweyDivision of Cardiovascular Medicine Stanford Cardiovascular Institute, Stanford University School of Medicine
Megan E GroveDivision of Cardiovascular Medicine Stanford Cardiovascular Institute, Stanford University School of Medicine
Marco V PerezDivision of Cardiovascular Medicine Stanford Cardiovascular Institute, Stanford University School of Medicine
Anne M DubinStanford University School of Medicine, Stanford University, California Stanford Cardiovascular Institute
Euan A AshleyDivision of Cardiovascular Medicine Child Health Research Institute Stanford Cardiovascular Institute, Stanford University School of Medicine
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