Idiopathic Restrictive Cardiomyopathy Is Primarily a Genetic Disease

Autor:	Félix Pérez-Villa, Luis Alonso-Pulpón, María Gallego-Delgado, Pablo García-Pavía, Joel Salazar-Mendiguchía, Esther Gonzalez-Lopez, Jesús Palomo, Raquel Marzoa-Rivas, Juan F. Delgado, Vicens Brossa-Loidi, Maria J. Ruiz-Cano, Belén Bornstein, Laura Padron-Barthe
Rok vydání:	2015
Předmět:	0301 basic medicine Adult Male medicine.medical_specialty Filamins Cardiomyopathy Disease 030204 cardiovascular system & hematology 03 medical and health sciences 0302 clinical medicine Internal medicine medicine Humans Cardiomyopathy Restrictive Myosin Heavy Chains business.industry Ventricular wall Restrictive cardiomyopathy Patient Acuity Sequence Analysis DNA Middle Aged medicine.disease 030104 developmental biology Heart Function Tests Cardiology Etiology End-diastolic volume Female Cardiology and Cardiovascular Medicine business Carrier Proteins Cardiac Myosins
Zdroj:	Journal of the American College of Cardiology. 67(25)
ISSN:	1558-3597
Popis:	Restrictive cardiomyopathy (RCM) is characterized by restrictive ventricular physiology in the presence of normal diastolic volume and normal ventricular wall thickness [(1)][1]. RCM is the least common cardiomyopathy and its prevalence is unknown [(1,2)][1]. Furthermore, its etiology could be
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::685a414da96057198a45d2c1e6ac34dd https://pubmed.ncbi.nlm.nih.gov/27339502 Zobrazit plný text záznamu