Mutations in ILK, encoding integrin linked kinase, are associated with arrhythmogenic cardiomyopathy

Arrhythmogenic cardiomyopathy is a genetic heart muscle disorder characterized by fibro-fatty replacement of cardiomyocytes leading to life-threatening ventricular arrhythmias, heart failure and sudden cardiac death. Mutations in genes encoding cardiac junctional proteins are known to cause about ha...

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Pubblicato in:Transl Res
Autori principali: Brodehl, Andreas, Rezazadeh, Saman, Williams, Tatjana, Munsie, Nicole M., Liedtke, Daniel, Oh, Tracey, Ferrier, Raechel, Shen, Yaoqing, Jones, Steven J. M., Stiegler, Amy L., Boggon, Titus J., Duff, Henry J., Friedman, Jan M., Gibson, William T., Childs, Sarah J., Gerull, Brenda
Natura: Artigo
Lingua:Inglês
Pubblicazione: 2019
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Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7412573/
https://ncbi.nlm.nih.gov/pubmed/30802431
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.trsl.2019.02.004
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