Ankyrin-B dysfunction predisposes to arrhythmogenic cardiomyopathy and is amenable to therapy

Arrhythmogenic cardiomyopathy (ACM) is an inherited arrhythmia syndrome characterized by severe structural and electrical cardiac phenotypes, including myocardial fibrofatty replacement and sudden cardiac death. Clinical management of ACM is largely palliative, owing to an absence of therapies that...

Szczegółowa specyfikacja

Zapisane w:
Opis bibliograficzny
Wydane w:J Clin Invest
Główni autorzy: Roberts, Jason D., Murphy, Nathaniel P., Hamilton, Robert M., Lubbers, Ellen R., James, Cynthia A., Kline, Crystal F., Gollob, Michael H., Krahn, Andrew D., Sturm, Amy C., Musa, Hassan, El-Refaey, Mona, Koenig, Sara, Aneq, Meriam Åström, Hoorntje, Edgar T., Graw, Sharon L., Davies, Robert W., Rafiq, Muhammad Arshad, Koopmann, Tamara T., Aafaqi, Shabana, Fatah, Meena, Chiasson, David A., Taylor, Matthew R.G., Simmons, Samantha L., Han, Mei, van Opbergen, Chantal J.M., Wold, Loren E., Sinagra, Gianfranco, Mittal, Kirti, Tichnell, Crystal, Murray, Brittney, Codima, Alberto, Nazer, Babak, Nguyen, Duy T., Marcus, Frank I., Sobriera, Nara, Lodder, Elisabeth M., van den Berg, Maarten P., Spears, Danna A., Robinson, John F., Ursell, Philip C., Green, Anna K., Skanes, Allan C., Tang, Anthony S., Gardner, Martin J., Hegele, Robert A., van Veen, Toon A.B., Wilde, Arthur A.M., Healey, Jeff S., Janssen, Paul M.L., Mestroni, Luisa, van Tintelen, J. Peter, Calkins, Hugh, Judge, Daniel P., Hund, Thomas J., Scheinman, Melvin M., Mohler, Peter J.
Format: Artigo
Język:Inglês
Wydane: American Society for Clinical Investigation 2019
Hasła przedmiotowe:
Research Article
Dostęp online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6668697/
https://ncbi.nlm.nih.gov/pubmed/31264976
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI125538
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