Absence of coding mutations in the X-lin
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Francesca Blasi; Elena Bacchelli; Giulia Pesaresi; Simona Carone; Anthony J. Bai
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Article
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2006
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John Wiley and Sons
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English
β 43 KB
π 2 views
## Abstract Neuroligin abnormalities have been recently implicated in the aetiology of autism spectrum disorders (ASD), given the finding of point mutations in the two Xβlinked genes NLGN3 and NLGN4X and the important role of neuroligins in synaptogenesis. To enquire on the relevance and frequency