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Disorders with similar clinical phenotypes reveal underlying genetic interaction: SATB2 acts as an activator of the UPF3B gene |
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| Authors: | Petcharat Leoyklang Kanya Suphapeetiporn Chalurmpon Srichomthong Siraprapa Tongkobpetch Stefanie Fietze Heidi Dorward Andrew R Cullinane William A Gahl Marjan Huizing Vorasuk Shotelersuk |
| Institution: | 1. Biomedical Science Program, Faculty of Graduate School, Chulalongkorn University, Bangkok, Thailand 2. Department of Pediatrics, Faculty of Medicine, The Center of Excellence for Medical Genetics, Chulalongkorn University, Bangkok, Thailand 3. Excellence Center for Medical Genetics, King Chulalongkorn Memorial Hospital, Thai Red Cross Society, Bangkok, Thailand 4. Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, 10 Center Drive, Building 10, Room 10C103, Bethesda, MD, 20892-1851, USA 6. Division of Medical Genetics and Metabolism, Department of Pediatrics, King Chulalongkorn Memorial Hospital, Sor Kor Building 11th Floor, Bangkok, 10330, Thailand 5. Department of Cellular and Molecular Immunology, Max Planck Institute of Immunobiology and Epigenetics, 79108, Freiburg, Germany |
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| 本文献已被 SpringerLink 等数据库收录！ | |