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Open Access
Peer-reviewed
Research Article
Mutations in SLC29A3, Encoding an Equilibrative Nucleoside Transporter ENT3, Cause a Familial Histiocytosis Syndrome (Faisalabad Histiocytosis) and Familial Rosai-Dorfman Disease
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Neil V. Morgan,
Affiliation Wellchild Paediatric Research Centre and Department of Medical and Molecular Genetics, University of Birmingham College of Medical and Dental Sciences, Edgbaston, Birmingham, United Kingdom
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Mark R. Morris,
Affiliations Wellchild Paediatric Research Centre and Department of Medical and Molecular Genetics, University of Birmingham College of Medical and Dental Sciences, Edgbaston, Birmingham, United Kingdom, Cancer Research UK Renal Molecular Oncology Group, Department of Medical and Molecular Genetics, University of Birmingham College of Medical and Dental Sciences, Edgbaston, Birmingham, United Kingdom
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Hakan Cangul,
Affiliations Wellchild Paediatric Research Centre and Department of Medical and Molecular Genetics, University of Birmingham College of Medical and Dental Sciences, Edgbaston, Birmingham, United Kingdom, Department of Medical Genetics, Uludag University School of Medicine, Bursa, Turkey
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Diane Gleeson,
Affiliation The Wellcome Trust Sanger Institute, Cambridge, United Kingdom
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Anna Straatman-Iwanowska,
Affiliation Wellchild Paediatric Research Centre and Department of Medical and Molecular Genetics, University of Birmingham College of Medical and Dental Sciences, Edgbaston, Birmingham, United Kingdom
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Nicholas Davies,
Affiliation School of Biosciences, University of Birmingham School of Medicine, Birmingham, United Kingdom
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Stephen Keenan,
Affiliations The Wellcome Trust Sanger Institute, Cambridge, United Kingdom, European Bioinformatics Institute, Cambridge, United Kingdom
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Shanaz Pasha,
Affiliation Wellchild Paediatric Research Centre and Department of Medical and Molecular Genetics, University of Birmingham College of Medical and Dental Sciences, Edgbaston, Birmingham, United Kingdom
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Fatimah Rahman,
Affiliation Wellchild Paediatric Research Centre and Department of Medical and Molecular Genetics, University of Birmingham College of Medical and Dental Sciences, Edgbaston, Birmingham, United Kingdom
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Dean Gentle,
Affiliations Wellchild Paediatric Research Centre and Department of Medical and Molecular Genetics, University of Birmingham College of Medical and Dental Sciences, Edgbaston, Birmingham, United Kingdom, Cancer Research UK Renal Molecular Oncology Group, Department of Medical and Molecular Genetics, University of Birmingham College of Medical and Dental Sciences, Edgbaston, Birmingham, United Kingdom
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Maaike P. G. Vreeswijk,
Affiliation Department of Human Genetics, Center for Human and Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands
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Peter Devilee,
Affiliations Department of Human Genetics, Center for Human and Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands, Clinical Genetics and the Department of Pathology, Leiden University Medical Center, Leiden, The Netherlands
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Margaret A. Knowles,
Affiliation Cancer Research UK Clinical Centre, Leeds Institute for Molecular Medicine, St James's University Hospital, Leeds, United Kingdom
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Serdar Ceylaner,
Affiliation Medical Genetics Intergen Genetics Centre, Ankara, Turkey
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Richard C. Trembath,
Affiliation Department of Medical and Molecular Genetics, King's College London School of Medicine, Guy's Hospital, London, United Kingdom
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Carlos Dalence,
Affiliation Division of Paediatric Haematology/Oncology, St. Joseph Children's Hospital, Tampa, Florida, United States of America
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Erol Kismet,
Affiliation Department of Pediatric Oncology, Gulhane Military Medical Academy, Ankara, Turkey
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Vedat Köseoğlu,
Affiliation Department of Pediatric Oncology, Gulhane Military Medical Academy, Ankara, Turkey
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Hans-Christoph Rossbach,
Affiliation Division of Paediatric Haematology/Oncology, St. Joseph Children's Hospital, Tampa, Florida, United States of America
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Paul Gissen,
Affiliation Wellchild Paediatric Research Centre and Department of Medical and Molecular Genetics, University of Birmingham College of Medical and Dental Sciences, Edgbaston, Birmingham, United Kingdom
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David Tannahill,
Affiliations The Wellcome Trust Sanger Institute, Cambridge, United Kingdom, Cranfield Health, Cranfield University, Bedford, United Kingdom
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Eamonn R. Maher
* E-mail: e.r.maher@bham.ac.uk
Affiliations Wellchild Paediatric Research Centre and Department of Medical and Molecular Genetics, University of Birmingham College of Medical and Dental Sciences, Edgbaston, Birmingham, United Kingdom, Cancer Research UK Renal Molecular Oncology Group, Department of Medical and Molecular Genetics, University of Birmingham College of Medical and Dental Sciences, Edgbaston, Birmingham, United Kingdom, West Midlands Region Genetics Service, Birmingham Women's Hospital, Edgbaston, United Kingdom
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Mutations in SLC29A3, Encoding an Equilibrative Nucleoside Transporter ENT3, Cause a Familial Histiocytosis Syndrome (Faisalabad Histiocytosis) and Familial Rosai-Dorfman Disease
- Neil V. Morgan,
- Mark R. Morris,
- Hakan Cangul,
- Diane Gleeson,
- Anna Straatman-Iwanowska,
- Nicholas Davies,
- Stephen Keenan,
- Shanaz Pasha,
- Fatimah Rahman,
- Dean Gentle

- Published: February 5, 2010
- https://doi.org/10.1371/journal.pgen.1000833