Whole‐Exome Sequencing Identifies a Rare <i>CSRP3</i> Variant Associated With Familial Brugada Syndrome in a Lebanese Family

Zainab Bashir, Ayat Kadhi, Jad Ballout, Bushra Samara, Maurice Khoury, Georges Nemer, Marwan Refaat

Open source

DOI: 10.1111/jce.70546
Published: 2026-10-29
Container: Journal of Cardiovascular Electrophysiology
Publisher: Wiley
Open access: unknown

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Cite this work

BibTeX

@article{allodium:10.1111/jce.70546,
  title = {Whole‐Exome Sequencing Identifies a Rare
                    <i>CSRP3</i>
                    Variant Associated With Familial Brugada Syndrome in a Lebanese Family},
  author = {Zainab Bashir and Ayat Kadhi and Jad Ballout and Bushra Samara and Maurice Khoury and Georges Nemer and Marwan Refaat},
  year = {2026},
  journal = {Journal of Cardiovascular Electrophysiology},
  doi = {10.1111/jce.70546},
  url = {https://doi.org/10.1111/jce.70546}
}

RIS

TY  - JOUR
TI  - Whole‐Exome Sequencing Identifies a Rare
                    <i>CSRP3</i>
                    Variant Associated With Familial Brugada Syndrome in a Lebanese Family
AU  - Zainab Bashir
AU  - Ayat Kadhi
AU  - Jad Ballout
AU  - Bushra Samara
AU  - Maurice Khoury
AU  - Georges Nemer
AU  - Marwan Refaat
PY  - 2026
JO  - Journal of Cardiovascular Electrophysiology
DO  - 10.1111/jce.70546
UR  - https://doi.org/10.1111/jce.70546
ER  -

APA

Bashir, Z., Kadhi, A., Ballout, J., Samara, B., Khoury, M., Nemer, G., & Refaat, M. (2026). Whole‐Exome Sequencing Identifies a Rare <i>CSRP3</i> Variant Associated With Familial Brugada Syndrome in a Lebanese Family. Journal of Cardiovascular Electrophysiology. https://doi.org/10.1111/jce.70546

Source records

crossref · retrieved 2026-11-10T13:40:44.140Z