Novel de novo SHANK3 mutation in autistic patients-Reference-Cited by-同舟云学术

Novel de novo SHANK3 mutation in autistic patients

Published:2009-04-05 Issue:3 Volume:150B Page:421-424
ISSN:1552-4841
Container-title:American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Gauthier Julie,Spiegelman Dan,Piton Amélie,Lafrenière Ronald G.,Laurent Sandra,St-Onge Judith,Lapointe Line,Hamdan Fadi F.,Cossette Patrick,Mottron Laurent,Fombonne Éric,Joober Ridha,Marineau Claude,Drapeau Pierre,Rouleau Guy A.

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Psychiatry and Mental health,Genetics(clinical)

Reference8 articles.

1. Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders;Durand;Nat Genet,2007

2. NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population;Gauthier;Am J Med Genet B Neuropsychiatr Genet,2005

3. Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism;Jamain;Nat Genet,2003

4. Neuropathology of infantile autism;Kemper;J Neuropathol Exp Neurol,1998

5. Contribution of SHANK3 Mutations to Autism Spectrum Disorder;Moessner;Am J Hum Genet,2007

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