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Duplication of the MECP2 Region Is a Frequent Cause of Severe Mental Retardation and Progressive Neurological Symptoms in Males

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Year: 2005
Type: article
Study design: Observational Study
Source: The American Journal of Human Genetics
DOI: 10.1086/444549
Authors: Hilde Van Esch, Marijke Bauters, Jaakko Ignatius, Mieke Jansen, Martine Raynaud, Karen Hollanders, Dorien Lugtenberg, Thierry Bienvenu, Lars Riff Jensen, Jozef Gécz, Claude Moraine, Peter Marynen, Jean-Pierre Fryns, Guy Froyen
Institutions: Universitair Ziekenhuis Leuven, Oulu University Hospital, University of Oulu, Centre Hospitalier Universitaire de Tours, Centre National de la Recherche Scientifique, Inserm, Institut Cochin, Université Paris Descartes, Max Planck Institute for Molecular Genetics, Women's and Children's Hospital, The University of Adelaide
Language: English

Topic: Genetics and Neurodevelopmental Disorders
Subfield: Genetics
Field: Biochemistry, Genetics and Molecular Biology
Domain: Life Sciences
SDG: Good health and well-being

Open Access status: bronze
OpenAlex ID: W1964159332
FWCI: 14.46
Cites: 37
Cited by: 647
Related to: 9
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