NRXN1 deletions identified by array comparative genome hybridisation in a clinical case series – further understanding of the relevance of NRXN1 to neurodevelopmental disorders-Reference-Cited by-同舟云学术

NRXN1 deletions identified by array comparative genome hybridisation in a clinical case series – further understanding of the relevance of NRXN1 to neurodevelopmental disorders

Published:2013 Issue:1 Volume:1 Page:4
ISSN:2049-9256
Container-title:Journal of Molecular Psychiatry
language:en
Short-container-title:J Mol Psychiatry

Author:

Curran Sarah,Ahn Joo Wook,Grayton Hannah,Collier David A,Ogilvie Caroline Mackie

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience

Reference34 articles.

1. Activation of α-Latrotoxin Receptors in Neuromuscular Synapses Leads to a Prolonged Splash Acetylcholine Release

2. Neurexins: Synaptic Cell Surface Proteins Related to the α-Latrotoxin Receptor and Laminin

3. Neuroligin 1: A splice site-specific ligand for β-neurexins

4. Neuroligins and neurexins link synaptic function to cognitive disease

5. Neurexophilin Binding to α-Neurexins

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