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المؤلفون: Dofash, L., Monahan, G., Servián-Morilla, E., Rivas, E., Faiz, F., Sullivan, P., Oates, E., Clayton, J., Taylor, R., Davis, M., Beilharz, T., Laing, N., Cabrera-Serrano, M., Ravenscroft, G.

المصدر: In Neuromuscular Disorders October 2022 32 Supplement 1:S45-S45

المؤلفون: Dofash, L., Faiz, F., Servián-Morilla, E., Rivas, E., Sullivan, P., Oates, E., Clayton, J., Taylor, R., Davis, M., Laing, N., Cabrera-Serrano, M., Ravenscroft, G.

المصدر: In Neuromuscular Disorders October 2021 31 Supplement 1:S60-S60

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المؤلفون: Johari M; Harry Perkins Institute of Medical Research, Centre for Medical Research, University of Western Australia, Nedlands, Perth, Western Australia, Australia.; Folkhälsan Research Center, Helsinki, Finland.; Department of Medical and Clinical Genetics, Medicum, University of Helsinki, Helsinki, Finland., Topf A; The John Walton Muscular Dystrophy Research Centre, Translational and Clinical Research Institute, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK., Folland C; Harry Perkins Institute of Medical Research, Centre for Medical Research, University of Western Australia, Nedlands, Perth, Western Australia, Australia., Duff J; The John Walton Muscular Dystrophy Research Centre, Translational and Clinical Research Institute, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK., Dofash L; Harry Perkins Institute of Medical Research, Centre for Medical Research, University of Western Australia, Nedlands, Perth, Western Australia, Australia., Marti P; Neuromuscular Research Group, IIS La Fe and CIBERER U763, Hospital Universitari i Politècnic La Fe, Valencia, Spain., Robertson T; Anatomical Pathology, Queensland Pathology, Brisbane, Queensland, Australia.; School of Biomedical Sciences, University of Queensland, Brisbane, Queensland, Australia., Vilchez J; Neuromuscular Research Group, IIS La Fe and CIBERER U763, Hospital Universitari i Politècnic La Fe, Valencia, Spain., Cairns A; Neurosciences Department, Queensland Children's Hospital, Brisbane, Queensland, Australia., Harris E; The John Walton Muscular Dystrophy Research Centre, Translational and Clinical Research Institute, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK., Marini-Bettolo C; The John Walton Muscular Dystrophy Research Centre, Translational and Clinical Research Institute, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK., Hundallah K; Division of Pediatric Neurology, Department of Pediatric, Prince Sultan Military Medical City, Riyadh, Riyadh, Saudi Arabia., Alhashem AM; Division of clinical genetic and metabolic medicine, Department of Pediatric, Prince Sultan Military Medical City, Riyadh, Saudi Arabia., Al-Owain M; Department of Medical Genomics, Centre for Genomic Medicine, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.; College of Medicine, Alfaisal University, Riyadh, Saudi Arabia., Maroofian R; Department of Neuromuscular Disorders, Queen Square Institute of Neurology, University College London, London, UK., Ravenscroft G; Harry Perkins Institute of Medical Research, Centre for Medical Research, University of Western Australia, Nedlands, Perth, Western Australia, Australia gina.ravenscroft@perkins.uwa.edu.au., Straub V; The John Walton Muscular Dystrophy Research Centre, Translational and Clinical Research Institute, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle upon Tyne, UK.

المصدر: Journal of medical genetics [J Med Genet] 2024 Aug 28. Date of Electronic Publication: 2024 Aug 28.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: British Medical Association Country of Publication: England NLM ID: 2985087R Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1468-6244 (Electronic) Linking ISSN: 00222593 NLM ISO Abbreviation: J Med Genet Subsets: MEDLINE