Familial hypertrophic cardiomyopathy associated with a new mutation in gene MYBPC3-Reference-Cited by-同舟云学术

Familial hypertrophic cardiomyopathy associated with a new mutation in gene MYBPC3

Published:2017-01-27 Issue:3 Volume:5 Page:232-237
ISSN:2050-0904
Container-title:Clinical Case Reports
language:en
Short-container-title:Clin Case Rep

Author:

Aurensanz Clemente Esther¹^ORCID,Ayerza Casas Ariadna¹,García Lasheras Cecilia¹,Ramos Fuentes Feliciano¹,Bueno Martínez Ines¹,Pelegrín Díaz Juana²,Ruiz Frontera Pablo³,Montserrat Iglesias Lorenzo⁴

Affiliation:

1. Department of Pediatrics; HCU Lozano Blesa; Zaragoza Spain

2. Department of Cardiology; HCU Lozano Blesa; Zaragoza Spain

3. Intensive Care Unit; HU Miguel Servet; Zaragoza Spain

4. Scientific Department; Health in Code; A Coruña Spain

Publisher

Wiley

Subject

General Medicine

Reference19 articles.

1. Prevalence of HCM and long QT syndrome mutations in young sudden cardiac death-related cases;Allegue;Int. J. Legal Med.,2011

2. Clinical features and prognostic implications of familial hypertrophic cardiomyopathy related to the cardiac myosin binding protein C gene;Charron;Circulation,1998

3. Genetic counselling and testing in cardiomyopathies;Charron;Eur. Heart J.,2010

4. ESC Guidelines on diagnosis and management of hypertrophic cardiomyopathy;Elliott;Eur. Heart J.,2014

5. Cardiac myosin binding protein C: its role in physiology and disease;Flashman;Circ. Res.,2004

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1. Chromosomal microarray and whole‐exome sequence analysis in Taiwanese patients with autism spectrum disorder;Molecular Genetics & Genomic Medicine;2019-10-08

2. Impact of molecular diagnostics in an asymptomatic amateur athlete found to be affected by hypertrophic cardiomyopathy;Medicina dello Sport;2018-10

3. A novel compound heterozygous variant of the SLC12A3 gene in Gitelman syndrome pedigree;BMC Medical Genetics;2018-01-29