NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population
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Association of autism with polymorphisms in the paired-like homeodomain transcription factor 1 (PITX1) on chromosome 5q31: a candidate gene analysisAutistic phenotypes and genetic testing: state-of-the-art for the clinical geneticistThe genetics of autistic disorders and its clinical relevance: a review of the literatureGenetics of autism spectrum disorderMolecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disordersReduced social interaction and ultrasonic communication in a mouse model of monogenic heritable autism.A neuroligin-4 missense mutation associated with autism impairs neuroligin-4 folding and endoplasmic reticulum exportDirect measure of the de novo mutation rate in autism and schizophrenia cohortsCurrent developments in the genetics of autism: from phenome to genomeNeurexin-neuroligin signaling in synapse developmentNovel splice isoforms for NLGN3 and NLGN4 with possible implications in autismNew players tip the scales in the balance between excitatory and inhibitory synapses.Neuroligin-1 deletion results in impaired spatial memory and increased repetitive behavior.Clinical and Neurobiological Relevance of Current Animal Models of Autism Spectrum Disorders.Genetics of Autism Spectrum Disorder: Current Status and Possible Clinical ApplicationsThe role of glutamate and its receptors in autism and the use of glutamate receptor antagonists in treatment.Developing Medications Targeting Glutamatergic Dysfunction in Autism: Progress to DateA Subset of Autism-Associated Genes Regulate the Structural Stability of Neurons.Familial deletion within NLGN4 associated with autism and Tourette syndromeSynaptic proteins and receptors defects in autism spectrum disordersIdentification of rare X-linked neuroligin variants by massively parallel sequencing in males with autism spectrum disorderMinimal 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.[Genetic and brain structure anomalies in autism spectrum disorders. Towards an understanding of the aetiopathogenesis?].The genetics of autism: key issues, recent findings, and clinical implications.The Role of the Y Chromosome in Brain Function.Neuroligin-deficient mutants of C. elegans have sensory processing deficits and are hypersensitive to oxidative stress and mercury toxicity.A population genetic approach to mapping neurological disorder genes using deep resequencing.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.Lack of association between NLGN3, NLGN4, SHANK2 and SHANK3 gene variants and autism spectrum disorder in a Chinese population.Synaptic signaling and aberrant RNA splicing in autism spectrum disordersThe neurobiology of autism.Autism-lessons from the X chromosome.Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia.Regulatory domain or CpG site variation in SLC12A5, encoding the chloride transporter KCC2, in human autism and schizophreniaIdentification of Four Novel Synonymous Substitutions in the X-Linked Genes Neuroligin 3 and Neuroligin 4X in Japanese Patients with Autistic Spectrum Disorder.X linked mental retardation: a clinical guide.Autism spectrum disorders: molecular genetic advances.Behavioral phenotypes in males with XYY and possible role of increased NLGN4Y expression in autism features.
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P2860
NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population
description
2005 nî lūn-bûn
@nan
2005 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population
@ast
NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population
@en
NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population
@nl
type
label
NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population
@ast
NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population
@en
NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population
@nl
prefLabel
NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population
@ast
NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population
@en
NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population
@nl
P2093
P50
P3181
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P1476
NLGN3/NLGN4 gene mutations are not responsible for autism in the Quebec population
@en
P2093
Anna Bonnel
Judith St-Onge
Liliane Karemera
Ridha Joober
Sandra Laurent
P3181
P356
10.1002/AJMG.B.30066
P407
P577
2005-01-05T00:00:00Z