Mutations of the UPF3B gene, which encodes a protein widely expressed in neurons, are associated with nonspecific mental retardation with or without autism-Reference-Cited by-同舟云学术

Mutations of the UPF3B gene, which encodes a protein widely expressed in neurons, are associated with nonspecific mental retardation with or without autism

Published:2009-02-24 Issue:7 Volume:15 Page:767-776
ISSN:1359-4184
Container-title:Molecular Psychiatry
language:en
Short-container-title:Mol Psychiatry

Author:

Laumonnier F,Shoubridge C,Antar C,Nguyen L S,Van Esch H,Kleefstra T,Briault S,Fryns J P,Hamel B,Chelly J,Ropers H H,Ronce N,Blesson S,Moraine C,Gécz J,Raynaud M

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Molecular Biology

Link

http://www.nature.com/articles/mp200914.pdf

Reference37 articles.

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3. Chiurazzi P, Schwartz CE, Gecz J, Neri G . XLMR genes: update 2007. Eur J Hum Genet 2008; 16: 422–434.

4. Van Esch H, Bauters M, Ignatius J, Jansen M, Raynaud M, Hollanders K et al. Duplication of the MECP2 region is a frequent cause of severe mental retardation and progressive neurological symptoms in males. Am J Hum Genet 2005; 77: 442–453.

5. Froyen G, Van Esch H, Bauters M, Hollanders K, Frints SG, Vermeesch JR et al. Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: important role for increased gene dosage of XLMR genes. Hum Mutat 2007; 28: 1034–1042.

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