Genetic Burden of TNNI3K in Diagnostic Testing of Patients With Dilated Cardiomyopathy and Supraventricular Arrhythmias

BACKGROUND: Genetic variants in TNNI3K (troponin-I interacting kinase) have previously been associated with dilated cardiomyopathy (DCM), cardiac conduction disease, and supraventricular tachycardias. However, the link between TNNI3K variants and these cardiac phenotypes shows a lack of consensus co...

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Detalles Bibliográficos
Autores principales: Pham, Caroline, Andrzejczyk, Karolina, Jurgens, Sean J., Lekanne Deprez, Ronald, Palm, Kaylin C.A., Vermeer, Alexa M.C., Nijman, Janneke, Christiaans, Imke, Barge-Schaapveld, Daniela Q.C.M., van Dessel, Pascal F.H.M., Beekman, Leander, Choi, Seung Hoan, Lubitz, Steven A., Skoric-Milosavljevic, Doris, van den Bersselaar, Lisa, Jansen, Philip R., Copier, Jaël S., Ellinor, Patrick T., Wilde, Arthur A.M., Bezzina, Connie R., Lodder, Elisabeth M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10426786/
https://www.ncbi.nlm.nih.gov/pubmed/37199186
http://dx.doi.org/10.1161/CIRCGEN.122.003975

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10426786/
https://www.ncbi.nlm.nih.gov/pubmed/37199186
http://dx.doi.org/10.1161/CIRCGEN.122.003975

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