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- Publisher
- Wiley
- Copyright
- Copyright © 2006 Wiley‐Liss, Inc., A Wiley Company
- ISSN
- 1552-4841
- eISSN
- 1552-485X
- DOI
- 10.1002/ajmg.b.30287
- pmid
- 16508939
- Publisher site
- See Article on Publisher Site
Abstract
Neuroligin abnormalities have been recently implicated in the aetiology of autism spectrum disorders (ASD), given the finding of point mutations in the two X‐linked genes NLGN3 and NLGN4X and the important role of neuroligins in synaptogenesis. To enquire on the relevance and frequency of neuroligin mutations in ASD, we performed a mutation screening of NLGN3 and NLGN4X in a sample of 124 autism probands from the International Molecular Genetic Study of Autism Consortium (IMGSAC). We identified a new non‐synonymous variant in NLGN3 (Thr632Ala), which is likely to be a rare polymorphism. Our data indicate that coding mutations in these genes are very rarely associated to ASD. © 2006 Wiley‐Liss, Inc.
Journal
American Journal of Medical Genetics part B – Wiley
Published: Apr 5, 2006
Keywords: autism; neuroligin; chromosome X; mutation screening; synaptogenesis