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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Detalhes bibliográficos
Publicado no:Transl Res
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: 2019
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Article
Acesso em linha: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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