Absence of a Primary Role for SCN10A Mutations in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy

Prior reports have identified associations between SCN10A and cardiac disorders, such as atrial fibrillation and Brugada syndrome. We evaluated SCN10A in 151 probands with ARVD/C. In this cohort, 10 putatively pathogenic SCN10A variants were identified, including a novel frameshift insertion. Despit...

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Bibliografiska uppgifter
I publikationen:J Cardiovasc Transl Res
Huvudupphovsmän: te Riele, Anneline S. J. M., James, Cynthia A., Murray, Brittney, Tichnell, Crystal, Amat-Alarcon, Nuria, Burks, Kathleen, Tandri, Harikrishna, Calkins, Hugh, Polydefkis, Michael, Judge, Daniel P.
Materialtyp: Artigo
Språk:Inglês
Publicerad: 2016
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Article
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC7539289/
https://ncbi.nlm.nih.gov/pubmed/26733327
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12265-015-9670-0
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