CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders
about
De novo and rare inherited copy-number variations in the hemiplegic form of cerebral palsy.Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome.Structural abnormalities in the primary somatosensory cortex and a normal behavioral profile in Contactin-5 deficient mice.Intragenic CNTNAP2 Deletions: A Bridge Too Far?Disconnecting CNTNAP2.Mutations in RAB39B in individuals with intellectual disability, autism spectrum disorder, and macrocephaly.Allele-Specific Biased Expression of the CNTN6 Gene in iPS Cell-Derived Neurons from a Patient with Intellectual Disability and 3p26.3 Microduplication Involving the CNTN6 Gene.Cntn6 deficiency impairs allocentric navigation in mice.Induced pluripotent stem cells as a tool to study brain circuits in autism-related disorders
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P2860
CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disorders
description
2016 nî lūn-bûn
@nan
2016 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2016 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
name
CNTN6 mutations are risk facto ...... n in autism spectrum disorders
@ast
CNTN6 mutations are risk facto ...... n in autism spectrum disorders
@en
type
label
CNTN6 mutations are risk facto ...... n in autism spectrum disorders
@ast
CNTN6 mutations are risk facto ...... n in autism spectrum disorders
@en
prefLabel
CNTN6 mutations are risk facto ...... n in autism spectrum disorders
@ast
CNTN6 mutations are risk facto ...... n in autism spectrum disorders
@en
P2093
P2860
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P356
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CNTN6 mutations are risk facto ...... n in autism spectrum disorders
@en
P2093
A Beggiato
A Danckaert
A L Mosca-Boidron
B Régnault
C Gillberg
F Amsellem
G André-Leroux
P2860
P2888
P304
P356
10.1038/MP.2016.61
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P50
P577
2016-05-10T00:00:00Z