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    "Department of Medical BioSciences, Radboud University Medical Center, Nijmegen, The Netherlands",
    "LYOS INSERM1033 Research Unit, Department of Pediatric Nephrology, Rheumatology and Dermatology, Reference Center for Rare Renal Diseases, Reference Center for Rare Diseases of Phosphate and Calcium, Femme Mère Enfant Hospital, Hospices Civils de Lyon, Lyon, France",
    "Centre de Génétique Humaine, Institut de Pathologie et de Génétique, Gosselies, Belgium",
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    "Fondazione FIRMO Onlus (Italian Foundation for the Research on Bone Diseases), Florence, Italy",
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    "Division of Nephrology, Cliniques Universitaires Saint-Luc, Brussels, Belgium",
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    "Laboratoire des Maladies Rénales Héréditaires, Service de Néphrologie Pédiatrique Centre de Référence Maladies Rénales Héréditaires de l'Enfant et de l'Adulte (MARHEA), Hôpital Necker-Enfants Malades, Assistance Publique, Hôpitaux de Paris (AP-HP), Inserm UMR 1163, Institut Imagine, Université Paris Cité, Paris, France",
    "Endocrinology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy",
    "Department of Nephrology, Great Ormond Street Hospital for Children and UCL Great Ormond Street Institute of Child Health, London, UK",
    "NIHR Newcastle Biomedical Research Centre & Renal Services, Newcastle Hospitals NHS Foundation Trust, Biosciences Institute, Newcastle University, Newcastle upon Tyne, UK",
    "Department of General Pediatrics, Pediatric Nephrology, University Children’s Hospital, Münster, Germany",
    "Department of Nephrology, Radboud university medical center, Nijmegen, The Netherlands"
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      "origin": "journal-openalex:2727|Chronic Kidney Disease and Diabetes",
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  "title": "Hypomagnesemia in Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Syndrome Caused by Pathogenic Variants of GATA3",
  "title_text": "Hypomagnesemia in Hypoparathyroidism, Sensorineural Deafness, and Renal Dysplasia Syndrome Caused by Pathogenic Variants of GATA3",
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