Identification of two variants in <i>AGRN</i> and <i>RPL3L</i> genes in a patient with catecholaminergic polymorphic ventricular tachycardia suggesting new candidate disease genes and digenic inheritance-Reference-Cited by-同舟云学术

Identification of two variants in AGRN and RPL3L genes in a patient with catecholaminergic polymorphic ventricular tachycardia suggesting new candidate disease genes and digenic inheritance

Published:2022-02 Issue:2 Volume:10 Page:
ISSN:2050-0904
Container-title:Clinical Case Reports
language:en
Short-container-title:Clinical Case Reports

Author:

Jaouadi Hager¹²^ORCID,Chabrak Sonia³,Lahbib Saida¹,Abdelhak Sonia¹,Zaffran Stéphane²^ORCID

Affiliation:

1. Biomedical Genomics and Oncogenetics Laboratory LR16IPT05 Institut Pasteur de Tunis Tunis Tunisia

2. Aix Marseille Université INSERM, Marseille Medical Genetics Marseille France

3. Faculty of Medicine of Tunis Université Tunis El Manar Tunis Tunisia

Funder

Ministry of Higher Education and Scientific Research

Publisher

Wiley

Subject

General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ccr3.5339

Reference17 articles.

1. Clinical and Molecular Characterization of Patients With Catecholaminergic Polymorphic Ventricular Tachycardia

2. The clinical and genetic spectrum of catecholaminergic polymorphic ventricular tachycardia: findings from an international multicentre registry

3. Current topics in catecholaminergic polymorphic ventricular tachycardia

4. Update on genetics of catecholaminergic polymorphic ventricular tachycardia;Campuzano O;Med Res Arch,2018

5. Identification of a novel exon3 deletion of RYR2 in a family with catecholaminergic polymorphic ventricular tachycardia

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