Communicated by Mark H. Paalman
Mutations in SYNGAP1 Cause Intellectual Disability, Autism, and a Specific Form of Epilepsy by Inducing Haploinsufficiency
Version of Record online: 12 DEC 2012
© 2012 WILEY PERIODICALS, INC.
Volume 34, Issue 2, pages 385–394, February 2013
How to Cite
Berryer, M. H., Hamdan, F. F., Klitten, L. L., Møller, R. S., Carmant, L., Schwartzentruber, J., Patry, L., Dobrzeniecka, S., Rochefort, D., Neugnot-Cerioli, M., Lacaille, J.-C., Niu, Z., Eng, C. M., Yang, Y., Palardy, S., Belhumeur, C., Rouleau, G. A., Tommerup, N., Immken, L., Beauchamp, M. H., Patel, G. S., Majewski, J., Tarnopolsky, M. A., Scheffzek, K., Hjalgrim, H., Michaud, J. L. and Di Cristo, G. (2013), Mutations in SYNGAP1 Cause Intellectual Disability, Autism, and a Specific Form of Epilepsy by Inducing Haploinsufficiency. Hum. Mutat., 34: 385–394. doi: 10.1002/humu.22248
Contract grant sponsors: Canadian Institute of Health Research; Réseau de Médecine Génétique Appliquée; Scottish Rite Charitable Foundation; FORGE Canada.
- Issue online: 29 JAN 2013
- Version of Record online: 12 DEC 2012
- Accepted manuscript online: 15 NOV 2012 12:29PM EST
- Manuscript Accepted: 31 OCT 2012
- Manuscript Received: 15 JUN 2012
- Canadian Institute of Health Research
- Réseau de Médecine Génétique Appliquée
- Scottish Rite Charitable Foundation; FORGE Canada
- Danish National Research Foundation
- Lundbeck Foundation
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