Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment - Test2 - elhamkhani - TriplyDB

Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment

Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment

http://www.wikidata.org/entity/Q33601252

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Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders.TLDc proteins: new players in the oxidative stress response and neurological disease.Language and Cognitive Impairment Associated with a Novel p.Cys63Arg Change in the MED13L Transcriptional Regulator.A novel genetic syndrome with STARD9 mutation and abnormal spindle morphology.Narrowing the Genetic Causes of Language Dysfunction in the 1q21.1 Microduplication Syndrome.Sociability and synapse subtype-specific defects in mice lacking SRPX2, a language-associated gene.Toward the Language Oscillogenome

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Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment

http://www.wikidata.org/entity/Q33601252

description

2017 nî lūn-bûn

@nan

2017 թուականի Ապրիլին հրատարակուած գիտական յօդուած

@hyw

2017 թվականի ապրիլին հրատարակված գիտական հոդված

@hy

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

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

@yue

name

Next-generation DNA sequencing ...... n specific language impairment

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Next-generation DNA sequencing ...... n specific language impairment

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type

label

Next-generation DNA sequencing ...... n specific language impairment

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Next-generation DNA sequencing ...... n specific language impairment

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prefLabel

Next-generation DNA sequencing ...... n specific language impairment

@ast

Next-generation DNA sequencing ...... n specific language impairment

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Scientific Reports

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Next-generation DNA sequencing ...... n specific language impairment

@en

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Dianne F Newbury

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

Rose H Reader

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

Xiaowei Sylvia Chen

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

P2860

The axon guidance receptor gene ROBO1 is a candidate gene for developmental dyslexia

An integrated map of genetic variation from 1,092 human genomes

Gene ontology: tool for the unification of biology

DCDC2 is associated with reading disability and modulates neuronal development in the brain.

Increased expression of the dyslexia candidate gene DCDC2 affects length and signaling of primary cilia in neurons

DYX1C1 is required for axonemal dynein assembly and ciliary motility

A functional genetic link between distinct developmental language disorders

The human language-associated gene SRPX2 regulates synapse formation and vocalization in mice

A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States.

Rare structural variants found in attention-deficit hyperactivity disorder are preferentially associated with neurodevelopmental genes

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46105

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10.1038/SREP46105

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7

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Joris A Veltman

Nuala H Simpson

Alexander Hoischen

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2017-04-25T00:00:00Z

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1084955150

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28440294

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5404330

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