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                                       Details for article 10 of 30 found articles
 
 
  Genome sequencing in a genetically elusive multigenerational long QT syndrome pedigree identifies a novel LQT2-causative deeply intronic KCNH2 variant
 
 
Title: Genome sequencing in a genetically elusive multigenerational long QT syndrome pedigree identifies a novel LQT2-causative deeply intronic KCNH2 variant
Author: Tobert, Kathryn E.
Tester, David J.
Zhou, Wei
Haglund-Turnquist, Carla M.
Giudicessi, John R.
Ackerman, Michael J.
Appeared in: Heart rhythm
Paging: Volume 19 () nr. 6 pages 998-1007
Year: 2022
Contents:
Publisher: Heart Rhythm Society
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

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