Research Article
Published: 02 February, 2018 | Volume 3 - Issue 1 | Pages: 006-007
Founder mutations are rare causes in arrhythmogenic cardiomyopathy including TMEM43 und phospholamban mutations. The incidence is approximately 1%. P.S358L TMEM43 mutations cause aggressive, in most cases biventricular arrhythmogenic cardiomyopathy [1], with the necessity of primary prophylactic ICD implantation in men and in women>30 years for sudden cardiac death prevention.
Read Full Article HTML DOI: 10.29328/journal.jccm.1001021 Cite this Article Read Full Article PDF
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