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A novel mutation in the DLG3 gene encoding the synapse-associated protein 102 (SAP102) causes non-syndromic mental retardation

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Year: 2009
Type: article
Study design: Observational Study
Source: Neurogenetics
DOI: 10.1007/s10048-009-0224-y
Authors: Ginevra Zanni, Hilde van Esch, Anissa Bensalem, Yoann Saillour, Karine Poirier, Laetitia Castelnau, Hans Hilger Ropers, Arjan P. M. de Brouwer, Fréderic Laumonnier, Jean-Pierre Fryns, Jamel Chelly
Institutions: Centre National de la Recherche Scientifique, Inserm, Hôpital Cochin, Institut Cochin, Université Paris Descartes, Universitair Ziekenhuis Leuven, Université de Tours, Centre Hospitalier Universitaire de Tours, GREMAN, Matériaux, Microélectronique, Acoustique, Nanotechnologies, Max Planck Institute for Molecular Genetics, Radboud University Medical Center
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: closed
OpenAlex ID: W1972012799
FWCI: 2.671
Cites: 24
Cited by: 54
Related to: 10
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