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Journal Article
The Journal of clinical investigation, ISSN 0021-9738, 01/2013, Volume 123, Issue 1, pp. 19 - 26
.... Many mutations are "private" or rare variants, often unique to families. In contrast, dilated cardiomyopathy (DCM... 
Life Sciences & Biomedicine | Medicine, Research & Experimental | Science & Technology | Research & Experimental Medicine | Cardiomyopathy, Dilated - pathology | Humans | Heart Failure - physiopathology | Myosin Heavy Chains - genetics | Myosin Heavy Chains - metabolism | Arrhythmias, Cardiac - physiopathology | Sarcomeres - pathology | Arrhythmias, Cardiac - pathology | Mitochondria - genetics | Sarcomeres - genetics | Myocardium - metabolism | Heart Failure - etiology | Arrhythmias, Cardiac - genetics | Cardiac Myosins - metabolism | Arrhythmias, Cardiac - metabolism | Calcium-Binding Proteins - metabolism | Cardiomyopathy, Dilated - genetics | Cytoskeleton - pathology | Cardiomyopathy, Dilated - complications | Sarcomeres - metabolism | Cardiac Myosins - genetics | Cytoskeleton - genetics | Heart Failure - genetics | Myocardium - pathology | Arrhythmias, Cardiac - etiology | Heart Failure - metabolism | Mitochondria - metabolism | Heart Failure - pathology | Mitochondria - pathology | Cardiomyopathy, Dilated - metabolism | Carrier Proteins - genetics | Animals | Carrier Proteins - metabolism | Cardiomyopathy, Dilated - physiopathology | Cytoskeleton - metabolism | Mutation | Calcium-Binding Proteins - genetics | Gene mutations | Cardiomyopathy | Genetic aspects | Congestive heart failure | Diagnosis | Heart diseases | Genetic screening | Methods | Index Medicus | Abridged Index Medicus | Review Series
Journal Article
by Domínguez, Fernando and Cuenca, Sofía and Bilińska, Zofia and Toro, Rocío and Villard, Eric and Barriales-Villa, Roberto and Ochoa, Juan Pablo and Asselbergs, Folkert and Sammani, Arjan and Franaszczyk, Maria and Akhtar, Mohammed and Coronado-Albi, Maria José and Rangel-Sousa, Diego and Rodriguez-Palomares, Jose F and Jiménez-Jáimez, Juan and Garcia-Pinilla, José Manuel and Ripoll-Vera, Tomás and Mogollón-Jiménez, Maria Victoria and Fontalba-Romero, Ana and Garcia-Medina, Dolores and Palomino-Doza, Julian and de Gonzalo-Calvo, David and Cicerchia, Marcos and Salazar-Mendiguchia, Joel and Salas, Clara and Pankuweit, Sabine and Hey, Thomas Morris and Mogensen, Jens and Barton, Paul J and Charron, Philippe and Elliott, Perry and Garcia-Pavia, Pablo and Eiskjær, Hans and Barriales, Roberto and Fernández Fernández, Xusto and Cicerchia, Marcos and Monserrat, Lorenzo and Ochoa, Juan Pablo and Salazar-Mendiguchia, Joel and Mogollón, Maria Victoria and Ripoll, Tomás and Charron, Philippe and Richard, Pascale and Villard, Eric and Palomino Doza, Julian and Fontalba, Ana and Alonso-Pulpón, Luis and Cobo-Marcos, Marta and Domínguez, Fernando and Garcia-Pavia, Pablo and Gómez-Bueno, Manuel and González-López, Esther and Hernández-Hernández, Aitor and Hernández-Pérez, Francisco José and López-Sainz, Ángela and Restrepo-Córdoba, Alejandra and Segovia-Cubero, Javier and Toro, Rocio and de Gonzalo-Calvo, David and Rosa Longobardo, Félix and Limeres, Javier and Rodriguez-Palomares, Jose F and Garcia-Pinilla, Jose Manuel and López-Garrido, Miguel A and Jiménez-Jaimez, Juan and Garcia-Medina, Dolores and Rangel Sousa, Diego and Peña, Maria Luisa and Mogensen, Jens and Morris-Hey, Thomas and Barton, Paul J and Cook, Stuart A and Midwinter, William and Roberts, Angharad M and Ware, James S and Walsh, Roddy and Akhtar, Mohammed and Elliott, Perry M and Rocha-Lopes, Luis and Savvatis, Konstantinos and Syrris, Petros and Michalak, Ewa and Ploski, Rafal and Sobieszczanska-Malek, Malgorzata and Bilińska, Zofia and Pankuweit, Sabine and Asselbergs, Folkert and Baas, Annette and Dooijes, Dennis and Sammani, Arjan and European Genetic Cardiomyopathies Initiative Investigators and European Genetic Cardiomyopathies
Journal of the American College of Cardiology, ISSN 0735-1097, 11/2018, Volume 72, Issue 20, pp. 2471 - 2481
.... Mutations in BAG3 are associated with dilated cardiomyopathy (DCM), but only a small number of cases have been reported to date, and the natural history of BAG3 cardiomyopathy is poorly understood... 
genetics | BAG3 | prognosis | dilated cardiomyopathy | Journal Article | Cardiac & Cardiovascular Systems | Life Sciences & Biomedicine | Cardiovascular System & Cardiology | Science & Technology | Cardiomyopathy, Dilated - genetics | Follow-Up Studies | Humans | Middle Aged | Heart Failure - genetics | Male | Mutation - genetics | Electrocardiography - statistics & numerical data | Young Adult | Cardiomyopathy, Dilated - physiopathology | Adaptor Proteins, Signal Transducing - genetics | Adolescent | Apoptosis Regulatory Proteins - genetics | Adult | Cardiomyopathy, Dilated - diagnosis | Female | Heart Failure - diagnosis | Cohort Studies | Analysis | Genetic aspects | Cardiomyopathy, Dilated | Immunohistochemistry | Heart | Arrhythmia | Syngeneic grafts | Cardiomyopathy | Genomics | Genes | Sex | Cardiovascular disease | Transplantation | Males | Kinases | Proteins | Ultrasonic imaging | Sinuses | Electrocardiography | Localization | Heart diseases | Relocation | Age | Deoxyribonucleic acid--DNA | Evaluation | Phenotypes | Statistical analysis | Heart transplantation | Patients | Dilated cardiomyopathy | Mutation | Ventricle | Index Medicus | Abridged Index Medicus | BAG3, BCL2-associated athanogene 3 | LVEF, left ventricular ejection fraction | SCD, sudden cardiac death | DCM, dilated cardiomyopathy | ICD, implantable cardioverter-defibrillator | IQR, interquartile range | VF, ventricular fibrillation | SVT, sustained ventricular tachycardia | LVAD, left ventricular assist device | LVEDD, left ventricular end-diastolic diameter | HTx, heart transplantation | HF, heart failure | ECG, electrocardiogram | NYHA, New York Heart Association
Journal Article
JAMA : the journal of the American Medical Association, ISSN 0098-7484, 03/2013, Volume 309, Issue 9, pp. 896 - 908
Journal Article