المؤلفون: Rita Rinaldi, Maria Letizia Bacchi Reggiani, Maddalena Graziosi, Raffaello Ditaranto, Giovanna Lattanzi, Matteo Ziacchi, Giovanni Vitale, Mauro Biffi, Giuseppe Boriani, Ferdinando Pasquale, Luciano Potena, Massimiliano Lorenzini, Alessandra Berardini, Claudio Rapezzi, Sofia Martin Suarez, Elena Biagini

المساهمون: Ditaranto, Raffaello, Boriani, Giuseppe, Biffi, Mauro, Lorenzini, Massimiliano, Graziosi, Maddalena, Ziacchi, Matteo, Pasquale, Ferdinando, Vitale, Giovanni, Berardini, Alessandra, Rinaldi, Rita, Lattanzi, Giovanna, Potena, Luciano, Martin Suarez, Sofia, Bacchi Reggiani, Maria Letizia, Rapezzi, Claudio, Biagini, Elena

المصدر: Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-11 (2019)
Orphanet Journal of Rare Diseases

مصطلحات موضوعية: Male, 0301 basic medicine, Ventricular Tachyarrhythmias, medicine.medical_treatment, Neuromuscular disorder, Cardiomyopathy, lcsh:Medicine, Laminopathy, 030204 cardiovascular system & hematology, Electrocardiography, 0302 clinical medicine, Pharmacology (medical), Prospective Studies, Child, Genetics (clinical), Heart transplantation, Heart, Atrial fibrillation, Neuromuscular Diseases, General Medicine, Middle Aged, Lamin Type A, Ventricular tachycardias, Natural history, Cardiology, Female, Adult, Familial cardiomyopathies, medicine.medical_specialty, Adolescent, Familial cardiomyopathie, Mutation, Missense, NO, Young Adult, 03 medical and health sciences, Internal medicine, medicine, Humans, Bradyarrhythmias, Emerin, Lamin, Neuromuscular disorders, In patient, Retrospective Studies, business.industry, Research, lcsh:R, medicine.disease, Bradyarrhythmia, 030104 developmental biology, Laminin, Cardiac phenotype, business

وصف الملف: STAMPA

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92d4c4f1694e746e141cb412726e4c9a
https://doi.org/10.1186/s13023-019-1245-8