Novel variants in TECRL cause recessive inherited CPVT type 3 with severe and variable clinical symptoms-Reference-Cited by-同舟云学术

Novel variants in TECRL cause recessive inherited CPVT type 3 with severe and variable clinical symptoms

Published:2020-03-22 Issue:6 Volume:31 Page:1527-1535
ISSN:1045-3873
Container-title:Journal of Cardiovascular Electrophysiology
language:en
Short-container-title:J Cardiovasc Electrophysiol

Author:

Moscu‐Gregor Alexander¹^ORCID,Marschall Christoph¹,Müntjes Carsten²,Schönecker Anne²,Schuessler‐Hahn Franziska³,Hohendanner Felix³,Parwani Abdul Shokor³,Boldt Leif‐Hendrik³,Ott Claus‐Eric⁴,Bennewiz Anja⁵,Paul Thomas⁶,Krause Ulrich⁶,Rost Imma¹

Affiliation:

1. Department of Molecular GeneticsMVZ Martinsried GmbH Martinsried Germany

2. Department of Pediatric Cardiology, Clinic for Pediatrics IIIEssen University Hospital Essen Germany

3. Division of Cardiology, Medical DepartmentCharité Campus Virchow‐Klinikum Berlin Germany

4. Institute of Medical Genetics and Human Genetics Charité Berlin Germany

5. Praxis‐Kinderherz, Gesundheitszentrum Am Borsigturm Berlin Germany

6. Department of Pediatric Cardiology and Pediatric Intensive Care MedicineUniversity Medical Center/Göttingen Göttingen Germany

Publisher

Wiley

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

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