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- [3] Sudden cardiac death in a patient with lamin A/C mutation in the absence of dilated cardiomyopathy or conduction diseaseClinical Research in Cardiology, 2011, 100 : 547 - 551Philipp EhlermannStephanie LehrkeTheano PapavassiliuBenjamin MederMartin BorggrefeHugo A. KatusRainer Schimpf
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- [5] Novel lamin A/C mutations in idiopathic dilated cardiomyopathy and/or conduction diseaseJOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2003, 41 (06) : 152A - 152Avan Tintelen, PKaterberg, HBoven, LWiesfeld, AWilde, AAvan Langen, IMRossenbacker, Tvan den Berg, MPvan Veldhuisen, DJBuys, CHHofstra, RVos, Y
- [6] Familial dilated cardiomyopathy with conduction disease caused by a lamin A/C mutation: Efficacy of the cardiac resynchronization therapy with a defibrillatorCIRCULATION, 2007, 116 (16) : 476 - 476Makiyama, TakeruAkao, MasaharuShizuta, SatoshiDoi, TakahirciOhno, SeikoNishio, YukikoKimura, TakeshiHorie, MinoruKita, Toru
- [7] Outcomes of dilated cardiomyopathy in Lamin A/C mutation carriersEUROPEAN HEART JOURNAL, 2018, 39 : 1324 - 1324Vaikhanskaya, T. G.Sivitskaya, L. N.Kurushka, T. V.Danilenko, N. G.Levdanskiy, O. G.Davydenko, O. G.
- [8] Lamin A/C mutations in patients with dilated cardiomyopathy and conduction disease, ventricular dysrhythmia or family history of sudden deathEUROPEAN HEART JOURNAL, 2009, 30 : 544 - 544Ehlermann, P.Georgiev, K.Ivandic, B.Zeller, R.Pribe, R.Zugck, C.Remppis, A.Gruenig, E.Weichenhan, D.Katus, H. A.
- [9] Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system diseaseJOURNAL OF CARDIAC FAILURE, 2001, 7 (03) : 249 - 256Jakobs, PMHanson, ELCrispell, KAToy, WKeegan, HSchilling, KIcenogle, TBLitt, MHershberger, RE
- [10] A novel deletion mutation accompanied by a point mutation in Lamin A/C gene: Screened from a dilated cardiomyopathy familyPERFUSION-UK, 2023, 38 (04): : 826 - 836Jia, HaoSun, YongxinYao, WangchaoChen, ZhenhangYang, ShouguoWang, ChunshengLu, Shuyang