X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy (original) (raw)
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Acknowledgements
We thank J. Searle and B. Powell for advice; A. Brown for technical assistance; the patients' families for donating samples; and Galliera Genetic Bank Italian Telethon project C42 for the stored samples from family 4. This work was supported by the Department of Molecular and Medical Genetics at Oregon Health Sciences University (R.S.W.) and by Celltech Chiroscience (M.E.B., M.A., M.Mc., S.P. and F.R.).
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Authors and Affiliations
- Department of Molecular and Medical Genetics, L103A, Oregon Health Sciences University, Portland, Oregon, USA
Robert S. Wildin - Celltech Chiroscience, Inc., Bothell, Washington, USA
Fred Ramsdell, Mark McEuen, Sean Proll, Mark Appleby & Mary E. Brunkow - Department of Paediatrics and Child Health, Royal Children's Hospital, Brisbane, Australia
Jane Peake - Laboratory of Human Genetics, Galliera Hospital, Genoa, Italy
Francesca Faravelli, Lucia Perroni & Franca Dagna Bricarelli - Service d'Immunologie et d'Hématologie Pédiatriques, The Laboratory of Human Genetics of Infectious Diseases (JLC), and Pediatric Gastroenterology (OG), University Hospital Necker-Enfants Malades, Paris, France
Jean-Laurent Casanova & Olivier Goulet - Department of Pediatrics, Oregon Health Sciences University, Portland, Oregon, USA
Neil Buist - Medical Genetics Unit, Shaare Zedek Medical Center , Jerusalem, Israel
Ephrat Levy-Lahad - Department of Neonatology, Neonatological Intensive Care Unit, G. Gaslini Institute, Genoa, Italy
Massimo Mazzella - Department of Endocrinology, Princess Margaret Hospital, Perth, Australia
Geoffrey Byrne
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Correspondence toRobert S. Wildin.
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Wildin, R., Ramsdell, F., Peake, J. et al. X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy.Nat Genet 27, 18–20 (2001). https://doi.org/10.1038/83707
- Received: 23 August 2000
- Accepted: 25 October 2000
- Issue Date: January 2001
- DOI: https://doi.org/10.1038/83707