Molecular characterization of Portuguese patients with dilated cardiomyopathy

Introduction: Dilated cardiomyopathy (DCM) is a disease of the heart muscle characterized by ventricular dilatation and impaired systolic function. Familial forms account for 30-50% of cases. Autosomal dominant inheritance is the predominant pattern of transmission. Causal genetic variants have been...

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Bibliographic Details
Main Author: Sousa, Alexandra (author)
Other Authors: Canedo, Paulo (author), Azevedo, Olga (author), Lopes, Luís (author), Pinho, Teresa (author), Baixia, Márcia (author), Rocha-Gonçalves, Francisco (author), Gonçalves, Lino (author), Cardoso, José Silva (author), Machado, José Carlos (author), Martins, Elisabete (author)
Format: article
Language:eng
Published: 2019
Subjects:
Dilated cardiomyopathy
Genetic variant
Next-generation sequencing
Miocardiopatia dilatada
Variante genética
Sequenciação massiva paralela
Adult
Cardiomyopathy, Dilated
Carrier Proteins
DNA
DNA Mutational Analysis
Echocardiography
Electrocardiography
Female
Genetic Markers
Genetic Variation
Heart Ventricles
Humans
Lamin Type A
Male
Phenotype
Portugal
Retrospective Studies
Troponin T
Mutation
Online Access:http://hdl.handle.net/10316/101607
Country:Portugal
Oai:oai:estudogeral.sib.uc.pt:10316/101607

Internet

http://hdl.handle.net/10316/101607

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