No evidence for involvement of genetic variants in the X-linked neuroligin genes NLGN3 and NLGN4X in probands with autism spectrum disorder on high functioning level
about
Autistic phenotypes and genetic testing: state-of-the-art for the clinical geneticistA neuroligin-4 missense mutation associated with autism impairs neuroligin-4 folding and endoplasmic reticulum exportThe role of glutamate and its receptors in autism and the use of glutamate receptor antagonists in treatment.Sex chromosome abnormalities and psychiatric diseasesA Subset of Autism-Associated Genes Regulate the Structural Stability of Neurons.Neurexins and neuroligins: synapses look out of the nervous systemSynaptic proteins and receptors defects in autism spectrum disordersAssociation study of SHANK3 gene polymorphisms with autism in Chinese Han population.Minimal aberrant behavioral phenotypes of neuroligin-3 R451C knockin miceAutism Genetic Database (AGD): a comprehensive database including autism susceptibility gene-CNVs integrated with known noncoding RNAs and fragile sites.The Role of the Y Chromosome in Brain Function.A sex-specific association of common variants of neuroligin genes (NLGN3 and NLGN4X) with autism spectrum disorders in a Chinese Han cohort.Efficient strategy for the molecular diagnosis of intellectual disability using targeted high-throughput sequencing.Drosophila neuroligin3 regulates neuromuscular junction development and synaptic differentiation.Klinefelter syndrome as a window on the aetiology of language and communication impairments in children: the neuroligin-neurexin hypothesis.Links between genetics and pathophysiology in the autism spectrum disorders.Identification of Four Novel Synonymous Substitutions in the X-Linked Genes Neuroligin 3 and Neuroligin 4X in Japanese Patients with Autistic Spectrum Disorder.Association Analysis of Noncoding Variants in Neuroligins 3 and 4X Genes with Autism Spectrum Disorder in an Italian CohortPentapeptide sharing between Corynebacterium diphtheria toxin and the human neural protein network.
P2860
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P2860
No evidence for involvement of genetic variants in the X-linked neuroligin genes NLGN3 and NLGN4X in probands with autism spectrum disorder on high functioning level
description
2008 nî lūn-bûn
@nan
2008 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
No evidence for involvement of ...... rder on high functioning level
@ast
No evidence for involvement of ...... rder on high functioning level
@en
No evidence for involvement of ...... rder on high functioning level
@nl
type
label
No evidence for involvement of ...... rder on high functioning level
@ast
No evidence for involvement of ...... rder on high functioning level
@en
No evidence for involvement of ...... rder on high functioning level
@nl
prefLabel
No evidence for involvement of ...... rder on high functioning level
@ast
No evidence for involvement of ...... rder on high functioning level
@en
No evidence for involvement of ...... rder on high functioning level
@nl
P50
P3181
P356
P1476
No evidence for involvement of ...... rder on high functioning level
@en
P2093
Anne-Kathrin Wermter
Inge Kamp-Becker
P3181
P356
10.1002/AJMG.B.30618
P407
P577
2008-06-05T00:00:00Z