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Comment
. 2022 Aug;19(8):504.
doi: 10.1038/s41569-022-00744-3.

Gene therapy for Brugada syndrome

Karina Huynh  1
Affiliations
Comment

Gene therapy for Brugada syndrome

Karina Huynh. Nat Rev Cardiol. 2022 Aug.
No abstract available

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References

Original article
    1. Yu, G. et al. Gene therapy targeting protein trafficking regulator MOG1 in mouse models of Brugada syndrome, arrhythmias, and mild cardiomyopathy. Sci. Transl. Med. 14, eabf3136 (2022) - DOI

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