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Mutations in ZBTB20 cause Primrose syndrome

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第一作者: Cordeddu,V.
作者单位: Department of Neurology, University of Cincinnati, Gardner Family Center for Parkinson's Disease [1] Medical Genetic Unit, SARAH Network of Rehabilitation Hospitals, Brasilia, Brazil [2] Department of Clinical Epidemiology,Biostatistics and Bioinformatics, Academic Medical Center [3] Dipartimento di Scienze Neurologiche,Neurochirurgiche e del Comportamento, Universita degli Studi [4] Podlaskie Center of Clinical Genetics, Bialystok, Poland [5] Dipartimento di Scienze e Tecnologie Chimiche, Universita 'Tor Vergata', Rome, Italy [6] Department of Pediatrics, Academic Medical Center, University of Amsterdam, Amsterdam, Netherlands [7] Clinical Genetics Department, Great Ormond Street Hospital, Children National Health Service (NHS [8] Dipartimento di Malattie Infettive,Parassitarie e Immunomediate, Istituto Superiore di Sanita, Rome [9] Dipartimento di Biologia Cellulare e Neuroscienze, Istituto Superiore di Sanita, Rome, Italy [10] Laboratorio Mendel, Fondazione Casa Sollievo della Sofferenza, San Giovanni Rotondo, Italy [11] Dipartimento di Ematologia,Oncologia e Medicina Molecolare, Istituto Superiore di Sanita, Rome [12] Dipartimento di Pediatria, Facolta di Medicina e Chirurgia, Universita 'Federico II', Naples, Italy [13] Department of Genome Analysis, Academic Medical Center, University of Amsterdam, Amsterdam [14] Department of Clinical Genetics, Academic Medical Center, University of Amsterdam, Amsterdam [15] Department of Medical Genetics, Children's Hospital of Pittsburgh, Pittsburgh, PA, United States [16] Department of Animal Breeding and Genetics, Swedish University of Agricultural Sciences, Uppsala [17]
发布时间 2014-11-25
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