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Characterization of ANKRD11 mutations in humans and mice related to KBG syndrome |
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| Authors: | Katherina Walz Devon Cohen Paul M Neilsen Joseph Foster II Francesco Brancati Korcan Demir Richard Fisher Michelle Moffat Nienke E Verbeek Kathrine Bjørgo Adriana Lo Castro Paolo Curatolo Giuseppe Novelli Clemer Abad Cao Lei Lily Zhang Oscar Diaz-Horta Juan I Young David F Callen Mustafa Tekin |
| Institution: | 1. Dr. John T. Macdonald Foundation Department of Human Genetics and John P. Hussman Institute for Human Genomics, Miller School of Medicine, University of Miami, 1501 NW 10 Ave, BRB 610, M-860, Miami, FL, 33136, USA 2. Department of Medicine, Miller School of Medicine, University of Miami, 1501 NW 10 Ave, BRB 418, M-860, Miami, FL, 33136, USA 3. Swinburne University of Technology Sarawak Campus, Kuching, Sarawak, Malaysia 4. Department of Medical, Oral and Biotechnological Sciences, Gabriele D’Annunzio University, 66100, Chieti, Italy 5. Medical Genetics Unit, Policlinico Tor Vergata University Hospital, Viale Oxford 81, 00133, Rome, Italy 6. Division of Pediatric Endocrinology, Dokuz Eylül University Faculty of Medicine, ?zmir, 35340, Turkey 7. Northern Genetics Service Teesside Genetics Unit, The James Cook University Hospital, Marton Road, Middlesbrough, TS4 3BW, UK 8. Department of Paediatric Dentistry, Newcastle Dental Hospital and School, Richardson Road, Newcastle upon Tyne, NE2 4AZ, UK 9. Department of Medical Genetics, University Medical Center Utrecht, Lundlaan 6, 3584 EA, Utrecht, The Netherlands 10. Department of Medical Genetics, Oslo University Hospital, Kirkeveien 166, 0450, Oslo, Norway 11. Department of Neuroscience, Pediatric Neurology and Psychiatry Unit, Tor Vergata University of Rome, 00165, Rome, Italy |
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