机译:Cardiac and pulmonary findings in dysferlinopathy: A 3‐year, longitudinal study
The Jain Foundation;
Center for Translational Science, Division of Biostatistics and Study Methodology,Children's;
Translational and Clinical Research Institute, Newcastle UniversityUniversity Paris‐Saclay, CEA, DRF, Service Hospitalier Frederic JoliotCharite Muscle Research Unit, Experimental and Clinical Research Center, a joint cooperation of theDepartment of Neurology and Neurological Sciences,Stanford University School of MedicineThe Children's Hospital at Westmead, and The University of SydneyDepartment of Neurology Children's National Health SystemService des maladies neuromusculaire et de la SLA, H?pital de La TimoneDepartment of Neurology Washington University School of MedicineFriedrich‐Baur‐Institute, Department of Neurology,Ludwig‐Maximilians‐University of MunichNeuromuscular Unit, Department of Neurology,Hospital U. Virgen del Rocío/Instituto de BiomedicinaCentre de référence des maladies neuromusculaires, Institut de Myologie, AP‐HP, Sorbonne UniversitDepartment of Neurology,National Center Hospital, National Center of Neurology and PsychiatryNeuroscience Institute, Carolinas Neuromuscular/ALS‐MDA Center, Carolinas HealthCare SystemDepartment of Neuroscience,University of PadovaThe Abigail Wexner Research Institute at Nationwide Children's HospitalThe John Walton Muscular Dystrophy Research Centre, Translational and Clinical Research InstituteCentro de Investigación Biomédica en Red en Enfermedades Raras (CIBERER)Department of Cardiology,Freeman Hospital, NUTH NHS Hospitals Foundation Trust;
cardiac; dysferlin; limb girdle muscular dystrophy R2; Miyoshi myopathy; respiratory;