'Unexpectedly Low Mutation Rates in beta-Myosin Heavy Chain and Cardiac Myosin Binding Protein Genes in Italian Patients with Hypertrophic Cardiomyopathy.'

Autor: Roberta Roncarati, 1, 2 Michael VG Latronico, 2 Beatrice Musumeci, 3 Stefania Aurino, 4 Annalaura Torella, 5 Marie-Louise Bang, 2, 6 Gloria Saccani Jotti, 7 Annibale A Puca, 2 Massimo Volpe, 3 Vincenzo Nigro, 4, 5 Camillo Autore, 3, Gianluigi Condorelli2, 8

Publikováno v: Journal of cellular physiology (Online) 226 (2011): 2894–2900. doi:10.1002/jcp.22636
info:cnr-pdr/source/autori:Roberta Roncarati,1,2 Michael VG Latronico,2 Beatrice Musumeci,3 Stefania Aurino,4 Annalaura Torella,5 Marie-Louise Bang,2,6 Gloria Saccani Jotti,7 Annibale A Puca,1,2 Massimo Volpe,3 Vincenzo Nigro,4,5 Camillo Autore,3 and Gianluigi Condorelli2,8,*/titolo:"Unexpectedly Low Mutation Rates in beta-Myosin Heavy Chain and Cardiac Myosin Binding Protein Genes in Italian Patients with Hypertrophic Cardiomyopathy."/doi:10.1002%2Fjcp.22636/rivista:Journal of cellular physiology (Online)/anno:2011/pagina_da:2894/pagina_a:2900/intervallo_pagine:2894–2900/volume:226
Journal of Cellular Physiology

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 (MYBP

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