Abstrakt
Atrial fibrillation (AF) is the most common sustained arrhythmia associated with several cardiac risk factors, but increasing evidences indicated a genetic component. Indeed, genetic variations of the atrial specific KCNA5 gene have been identified in patients with early-onset lone AF. To investigate the molecular mechanisms underlying AF, we reprogrammed to pluripotency polymorphonucleated leukocytes isolated from the blood of a patient carrying a KCNA5 p.D322H mutation, using a commercially available non-integrating system. The generated iPSCs expressed pluripotency markers and differentiated toward cells belonging to the three embryonic germ layers. Moreover, the cells showed a normal karyotype and retained the p.D322H mutation.
Originalsprog | Engelsk |
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Tidsskrift | Stem Cell Research |
Vol/bind | 24 |
Sider (fra-til) | 29-32 |
Antal sider | 4 |
ISSN | 1873-5061 |
DOI | |
Status | Udgivet - okt. 2017 |