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Disruption of MeCP2-TCF20 complex underlies distinct neurodevelopmental disorders.

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作者单位: Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030. [1] Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX 77030. [2] Department of Neuroscience, Baylor College of Medicine, Houston, TX 77030. [3] Department of Physiology and Immunology, College of Medicine and Health Sciences, Khalifa University of Science and Technology 127788 Abu Dhabi, United Arab Emirates. [4] Department of Pediatrics, Baylor College of Medicine, Houston, TX 77030. [5] US Department of Agriculture/Agricultural Research Service Children's Nutrition Research Center, Department of Pediatrics, Baylor College of Medicine, Houston, TX 77030. [6] Medical Scientist Training Program, Baylor College of Medicine, Houston, TX 77030. [7] Department of Pharmaceutical Chemistry, University of California, San Francisco, CA 94158. [8] HHMI, Baylor College of Medicine, Houston, TX 77030. [9] Program in Developmental Biology, Baylor College of Medicine, Houston, TX 77030. [10] HudsonAlpha Institute for Biotechnology, Huntsville, AL 35806. [11] Department of Neurology, University of Alabama at Birmingham, Birmingham, AL 35294. [12] Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen 72076, Germany. [13] Center for Rare Diseases, University of Tübingen, Tübingen 72076, Germany. [14] Institut für Humangenetik, Universitätsklinikum Essen, Essen 45147, Germany. [15] Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030; hzoghbi@bcm.edu. [16]
DOI 10.1073/pnas.2119078119
PMID 35074918
发布时间 2022-10-05
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Proceedings of the National Academy of Sciences of the United States of America

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