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Prevalence of cardiac beta-myosin heavy chain gene mutations in patients with hypertrophic cardiomyopathy

✍ Scribed by Andreas Perrot; Hajo Schmidt-Traub; Bernard Hoffmann; Matthias Prager; Nana Bit-Avragim; Raisa I. Rudenko; Dinara A. Usupbaeva; Zhyldyz Kabaeva; Bakytbek Imanov; Mirsaid M. Mirrakhimov; Heiko Witt; Rainer Dietz; Anna Wycisk; Michal Tendera; Reinhard Geßner; Karl Josef Osterziel

Publisher
Springer
Year
2005
Tongue
English
Weight
39 KB
Volume
83
Category
Article
ISSN
0946-2716

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Unexpectedly low mutation rates in beta-
Unexpectedly low mutation rates in beta-myosin heavy chain and cardiac myosin binding protein genes in italian patients with hypertrophic cardiomyopathy
✍ Roberta Roncarati; Michael V.G. Latronico; Beatrice Musumeci; Stefania Aurino; A 📂 Article 📅 2011 🏛 John Wiley and Sons 🌐 English ⚖ 138 KB

Hypertrophic cardiomyopathy (HCM) is the most common genetic cardiac disease. Fourteen sarcomeric and sarcomere-related genes have been implicated in HCM etiology, those encoding β-myosin heavy chain (__MYH7__) and cardiac myosin binding protein C (__MYBPC3__) reported as the most frequently mutated