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The recurrent de novo c.2011C>T missense variant in MTSS2 causes syndromic intellectual disability
Affiliation:1. Department of Molecular and Human Genetics, Baylor College of Medicine (BCM), Houston, TX 77030, USA;2. Jan and Dan Duncan Neurological Research Institute, Texas Children’s Hospital, Baylor College of Medicine, Houston, TX 77030, USA;3. Children’s Hospital of Eastern Ontario Research Institute, University of Ottawa, Ottawa, ON K1H 8L1, Canada;4. Broad Center for Mendelian Genomics, Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA 02142, USA;5. Division of Medical Genetics & Metabolism, Massachusetts General Hospital for Children, Boston, MA 02114, USA;6. Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA 02114, USA;7. Department of Pediatrics, Bethune International Peace Hospital, Shijiazhuang 050082, Hebei, China;8. Department of Clinical Genetics, Erasmus Medical Center, University Medical Center Rotterdam, Rotterdam, the Netherlands;9. Department of Neurology, Division of Neurogenetics, Child Neurology, Massachusetts General Hospital, Boston, MA 02114, USA;10. Department of Neurology, Boston Children’s Hospital, Boston, MA 02115, USA;11. Newborn Screening Ontario, Children’s Hospital of Eastern Ontario, Ottawa, ON K1H 8L1, Canada
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