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A novel hypomorphic MECP2 point mutation is associated with a neuropsychiatric phenotype
Authors:Abidemi A. Adegbola  Andrew Chess  Janine M. LaSalle  Gerald F. Cox
Affiliation:(1) Center for Human Genetic Research, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA;(2) Harvard Medical School, Boston, MA, USA;(3) Division of Genetics, Department of Medicine, Children’s Hospital Boston, Boston, MA, USA;(4) Medical Microbiology and Immunology, Rowe Program in Human Genetics, School of Medicine, University of California, Davis, CA, USA;(5) Department of Clinical Research, Genzyme Corporation, Cambridge, MA, USA;(6) Harvard-Partners Center for Genetics and Genomics, 77 Avenue Louis Pasteur, NRB 250, Boston, MA 02115, USA
Abstract:
Keywords:
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