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ISL1 loss-of-function variation causes familial atrial fibrillation
Affiliation:1. Radboud University Medical Centre, Donders Institute for Brain, Cognition and Behaviour, Centre for Cognitive Neuroscience, Department of Neurology, PO Box 9101, 6500 HB, Nijmegen, The Netherlands;2. Paris-Est Neuromuscular Center, Pitié-Salpêtrière Hospital, Paris, France;3. Biochemistry Department and Genetic Center, APHP, GHU Pitié-Salpêtrière, Paris, France;4. Unit of Neuromuscular Morphology, Institute of Myology, GHU La Pitié-Salpêtrière, Paris, France;5. Center for Inherited Metabolic Diseases, Hopital Necker Enfants Malades, AP-HP, University Paris Descartes, Paris, France;6. Institute of Myology, Pitié-Salpêtrière Hospital, 75651 Paris Cedex 13, France;7. Inserm U 1016, CNRS UMR 8104, Institut Cochin, Paris, France;8. GRC-UPMC Neuro-métabolisme, Université Pierre et Marie Curie, Paris, France;1. Department of Pediatrics, Faculty of Medicine, Chiang Mai University, Chiang Mai, 50200, Thailand;2. Department of Obstetrics and Gynecology, Faculty of Medicine, Chiang Mai University, Chiang Mai, 50200, Thailand
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