A human <it>MYBPC3</it> mutation appearing about 10 centuries ago results in a hypertrophic cardiomyopathy with delayed onset, moderate evolution but with a risk of sudden death

• Главные авторы: Teirlinck Carolien H (Автор), Senni Faïza (Автор), Malti Rajae El (Автор), Majoor-Krakauer Danielle (Автор), Fellmann Florence (Автор), Millat Gilles (Автор), André-Fouët Xavier (Автор), Pernot François (Автор), Stumpf Michaël (Автор), Boutarin Jean (Автор), Bouvagnet Patrice (Автор)
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• Опубликовано: BMC, 2012-11-01T00:00:00Z.
• Предметы: article
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<p>Abstract</p> <p>Background</p> <p>Hypertrophic Cardiomyopathy (HCM) is a genetically heterogeneous disease. One specific mutation in the <it>MYBPC3</it> gene is highly prevalent in center east of France giving an opportunity to define the clinical profile...