Duplication of the MECP2 Region Is a Frequent Cause of Severe Mental Retardation and Progressive Neurological Symptoms in Males
Year: 2005
Type: article
Study design: Observational Study
DOI: 10.1086/444549
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
Subfield: Genetics
Domain: Life Sciences
Open Access status: bronze
OpenAlex ID: W1964159332
