TBX5 ‐encoded T‐box transcription factor 5 variant T223M is associated with long QT syndrome and pediatric sudden cardiac death-Reference-Cited by-同舟云学术

TBX5 ‐encoded T‐box transcription factor 5 variant T223M is associated with long QT syndrome and pediatric sudden cardiac death

Published:2020-12-23 Issue:3 Volume:185 Page:923-929
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Markunas Alexandra M.¹,Manivannan Perathu K. R.¹,Ezekian Jordan E.¹,Agarwal Agnim²,Eisner William¹,Alsina Katherina³,Allen Hugh D.⁴,Wray Gregory A.²,Kim Jeffrey J.⁴,Wehrens Xander H. T.³,Landstrom Andrew P.¹⁵

Affiliation:

1. Department of Pediatrics, Division of Cardiology Duke University School of Medicine Durham North Carolina USA

2. Department of Biology Duke University Durham North Carolina USA

3. Departments of Molecular Physiology & Biophysics and Medicine (Cardiology) Baylor College of Medicine Houston Texas USA

4. Department of Pediatrics Section of Cardiology, Baylor College of Medicine Houston Texas USA

5. Department of Cell Biology Duke University School of Medicine Durham North Carolina USA

Funder

National Institutes of Health

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.62037

Reference40 articles.

1. HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies

2. An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome

3. A method and server for predicting damaging missense mutations

4. TBX5 drives Scn5a expression to regulate cardiac conduction system function

5. The Clinical and Genetic Spectrum of the Holt-Oram Syndrome (Heart-Hand Syndrome)

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