Screening mutations in myosin binding protein C3 gene in a cohort of patients with Hypertrophic Cardiomyopathy

• Main Authors: Maneiro Emilia (Author), Barriales-Villa Roberto (Author), Núñez Lucía (Author), Cazón Laura (Author), Fernández Xusto (Author), Ortiz Martín (Author), Monserrat Lorenzo (Author), Rodríguez-García María (Author), Veira Elena (Author), Castro-Beiras Alfonso (Author), Hermida-Prieto Manuel (Author)
• Format: Book
• Published: BMC, 2010-04-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

<p>Abstract</p> <p>Background</p> <p><it>MyBPC3 </it>mutations are amongst the most frequent causes of hypertrophic cardiomyopathy, however, its prevalence varies between populations. They have been associated with mild and late onset disease expression. Our...