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Homozygous single base deletion in TUSC3 causes intellectual disability with developmental delay in an Omani family
Authors:Ahmed Al‐Amri  Abeer Al Saegh  Watfa Al‐Mamari  Mohammed E. El‐Asrag  Jose L. Ivorra  Alastair G. Cardno  Chris F. Inglehearn  Steven J. Clapcote  Manir Ali
Affiliation:1. Section of Ophthalmology and Neuroscience, Leeds Institute of Biomedical and Clinical Sciences, University of Leeds, United Kingdom;2. School of Biomedical Sciences, University of Leeds, United Kingdom;3. National Genetic Centre, Directorate General of Royal Hospital, Ministry of Health, Muscat, Oman;4. Genetic and Developmental Medicine Clinic, Genetics Department, Sultan Qaboos University Hospital, Muscat, Oman;5. Developmental Pediatric Unit, Child Health Department, Sultan Qaboos University Hospital, Muscat, Oman;6. Department of Zoology, Faculty of Science, Benha University, Benha, Egypt;7. Academic Unit of Psychiatry and Behavioural Sciences, Leeds Institute of Health Sciences, University of Leeds, United Kingdom;8. Correspondence to:;9. Manir Ali, Ph.D., Section of Ophthalmology and Neuroscience, Leeds Institute of Biomedical and Clinical Sciences, Wellcome Trust Brenner Building, St. James's University Hospital, Leeds LS7 9TF, UK.;10. E‐mail:
Abstract:
Keywords:intellectual disability  exome sequencing  TUSC3
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