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Mutation screening of the MECP2 gene in a large cohort of 613 fragile-X negative patients with mental retardation
Authors:Lesca Gaëtan  Bernard Virginie  Bozon Muriel  Touraine Renaud  Gérard Daniel  Edery Patrick  Calender Alain
Affiliation:1. Division of Metabolic Disorders, CHOC Children''s Specialists, Orange, CA, USA;2. Department of Pediatrics, University of Minnesota Medical School, Minneapolis, MN, USA;3. Division of Biostatistics, University of Minnesota, School of Public Health, Minneapolis, MN, USA;4. School of Kinesiology, University of Minnesota, Minneapolis, MN, USA;1. Department of Basic Medical Science, Faculty of Medicine, Neyshabur University of Medical Science, Neyshabur, Iran;2. Medical Genetic Research Center (MGRC), School of Medicine, Mashhad University of Medical Sciences (MUMS), Mashhad, Iran;3. Human Genetics Division, Immunology Research Center, Avicenna Research Institute, Mashhad University of Medical Sciences (MUMS), Iran;1. CAS Key Laboratory for Biological Effects of Nanomaterials and Nanosafety, National Center for Nanoscience and Technology, No. 11 Zhongguancun Beiyitiao, Beijing 100190, China;2. The First Affiliated Hospital of Jilin University, Changchun 130021, China;3. Department of Hematology, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China;4. Department of Otorhinolaryngology, Peking University Third Hospital, Beijing 100191, China;1. Bionics Institute, Australia;2. Department of Medical Bionics, The University of Melbourne, Australia
Abstract:
Keywords:Mental retardation   MECP2   Mutation   Polymorphism   Molecular screening
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