Loss of Cntnap2 Causes Axonal Excitability Deficits, Developmental Delay in Cortical Myelination, and Abnormal Stereotyped Motor Behavior.

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Impact on birth weight of maternal smoking throughout pregnancy mediated by DNA methylation.Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies?

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P2860

Loss of Cntnap2 Causes Axonal Excitability Deficits, Developmental Delay in Cortical Myelination, and Abnormal Stereotyped Motor Behavior.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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Loss of Cntnap2 Causes Axonal ...... al Stereotyped Motor Behavior.

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Loss of Cntnap2 Causes Axonal ...... al Stereotyped Motor Behavior.

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Loss of Cntnap2 Causes Axonal ...... al Stereotyped Motor Behavior.

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Loss of Cntnap2 Causes Axonal ...... al Stereotyped Motor Behavior.

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Loss of Cntnap2 Causes Axonal ...... mal Stereotyped Motor Behavior

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P2093

Alberto Sánchez-Aguilera

http://www.w3.org/2001/XMLSchema#string

Elior Peles

http://www.w3.org/2001/XMLSchema#string

Giorgia Bartolini

http://www.w3.org/2001/XMLSchema#string

Hilgo Bruining

http://www.w3.org/2001/XMLSchema#string

Kim van Elst

http://www.w3.org/2001/XMLSchema#string

Martien J H Kas

http://www.w3.org/2001/XMLSchema#string

Ricardo Scott

http://www.w3.org/2001/XMLSchema#string

Sung Eun Bae

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P2860

Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.

Caspr2, a new member of the neurexin superfamily, is localized at the juxtaparanodes of myelinated axons and associates with K+ channels

Juxtaparanodal clustering of Shaker-like K+ channels in myelinated axons depends on Caspr2 and TAG-1

Functional disturbances within frontostriatal circuits across multiple childhood psychopathologies

Association of TAG-1 with Caspr2 is essential for the molecular organization of juxtaparanodal regions of myelinated fibers

Candidate autism gene screen identifies critical role for cell-adhesion molecule CASPR2 in dendritic arborization and spine development

Connectivity in Autism: A Review of MRI Connectivity Studies

Altered corpus callosum morphology associated with autism over the first 2 years of life.

Connecting the CNTNAP2 Networks with Neurodevelopmental Disorders

Synaptic, transcriptional and chromatin genes disrupted in autism

P304

586-597

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scholarly article

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10.1093/CERCOR/BHX341

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P478

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Nathalie Dehorter

Lynette Lim

Oscar Marin

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2019-02-01T00:00:00Z

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29300891

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Loss of Cntnap2 Causes Axonal Excitability Deficits, Developmental Delay in Cortical Myelination, and Abnormal Stereotyped Motor Behavior.

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P2860

P2860

Loss of Cntnap2 Causes Axonal Excitability Deficits, Developmental Delay in Cortical Myelination, and Abnormal Stereotyped Motor Behavior.

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