Human iPS cell model of type 3 long QT syndrome recapitulates drug-based phenotype correction

Long QT syndrome is a potentially life-threatening disease characterized by delayed repolarization of cardiomyocytes, QT interval prolongation in the electrocardiogram, and a high risk for sudden cardiac death caused by ventricular arrhythmia. The genetic type 3 of this syndrome (LQT3) is caused by...

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Kaydedildi:
Detaylı Bibliyografya
Yayımlandı:Basic Res Cardiol
Asıl Yazarlar: Malan, Daniela, Zhang, Miao, Stallmeyer, Birgit, Müller, Jovanca, Fleischmann, Bernd K., Schulze-Bahr, Eric, Sasse, Philipp, Greber, Boris
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Springer Berlin Heidelberg 2016
Konular:
Original Contribution
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4724360/
https://ncbi.nlm.nih.gov/pubmed/26803770
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00395-016-0530-0
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