Rare Variant in MRC2 Associated With Familial Supraventricular Tachycardia and Wolff-Parkinson-White Syndrome.

Potter AS, Miyake CY, Gonzaga-Jauregui C, Aguilar-Sanchez Y, Hulsurkar MM, Lahiri SK, Moreira LM, Mehta N, Azamian MS, Lupski JR, Reilly S, Lalani SR, Wehrens XHT

Open source

DOI: 10.1161/circgen.124.004614
Published: 2024 Aug
Container: Circulation. Genomic and precision medicine
Publisher: Not recorded
Open access: yes

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Cite this work

BibTeX

@article{allodium:10.1161/circgen.124.004614,
  title = {Rare Variant in MRC2 Associated With Familial Supraventricular Tachycardia and Wolff-Parkinson-White Syndrome.},
  author = {Potter AS and Miyake CY and Gonzaga-Jauregui C and Aguilar-Sanchez Y and Hulsurkar MM and Lahiri SK and Moreira LM and Mehta N and Azamian MS and Lupski JR and Reilly S and Lalani SR and Wehrens XHT},
  year = {2024},
  journal = {Circulation. Genomic and precision medicine},
  doi = {10.1161/circgen.124.004614},
  url = {https://doi.org/10.1161/circgen.124.004614}
}

RIS

TY  - JOUR
TI  - Rare Variant in MRC2 Associated With Familial Supraventricular Tachycardia and Wolff-Parkinson-White Syndrome.
AU  - Potter AS
AU  - Miyake CY
AU  - Gonzaga-Jauregui C
AU  - Aguilar-Sanchez Y
AU  - Hulsurkar MM
AU  - Lahiri SK
AU  - Moreira LM
AU  - Mehta N
AU  - Azamian MS
AU  - Lupski JR
AU  - Reilly S
AU  - Lalani SR
AU  - Wehrens XHT
PY  - 2024
JO  - Circulation. Genomic and precision medicine
DO  - 10.1161/circgen.124.004614
UR  - https://doi.org/10.1161/circgen.124.004614
ER  -

APA

AS, P., CY, M., C, G., Y, A., MM, H., SK, L., LM, M., N, M., MS, A., JR, L., S, R., SR, L., & XHT, W. (2024). Rare Variant in MRC2 Associated With Familial Supraventricular Tachycardia and Wolff-Parkinson-White Syndrome.. Circulation. Genomic and precision medicine. https://doi.org/10.1161/circgen.124.004614

Source records

pubmed · retrieved 2026-09-26T22:07:35.339Z
europe-pmc · retrieved 2026-09-26T22:07:35.352Z