Communicated by Stylianos E. Antonarakis
Exploring the potential role of disease-causing mutation in a gene desert: Duplication of noncoding elements 5′ of GRIA3 is associated with GRIA3 silencing and X-linked intellectual disability†
Article first published online: 28 NOV 2011
© 2011 Wiley Periodicals, Inc.
Volume 33, Issue 2, pages 355–358, February 2012
How to Cite
Bonnet, C., Masurel-Paulet, A., Khan, A. A., Béri-Dexheimer, M., Callier, P., Mugneret, F., Philippe, C., Thauvin-Robinet, C., Faivre, L. and Jonveaux, P. (2012), Exploring the potential role of disease-causing mutation in a gene desert: Duplication of noncoding elements 5′ of GRIA3 is associated with GRIA3 silencing and X-linked intellectual disability. Hum. Mutat., 33: 355–358. doi: 10.1002/humu.21649
- Issue published online: 12 JAN 2012
- Article first published online: 28 NOV 2011
- Manuscript Accepted: 1 NOV 2011
- Manuscript Received: 14 JUN 2011
- French Ministry of Health
- Fondation Jérome Lejeune
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