Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia (Q24649522)

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Language	Label	Description	Also known as
English	Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia	scientific article

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instance of

scholarly article

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title

Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia (English)

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main subject

developmental coordination disorder

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based on heuristic

inferred from title

developmental verbal dyspraxia

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based on heuristic

inferred from title

author

Sonja C Vernes

object named as

Sonja C Vernes

series ordinal

1

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Simon Fisher

object named as

Simon E Fisher

series ordinal

4

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Anthony Monaco

object named as

Anthony P Monaco

series ordinal

3

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author name string

Kay D MacDermot

series ordinal

2

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language of work or name

English

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publication date

October 2009

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published in

European Journal of Human Genetics

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volume

17

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issue

10

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page(s)

1354-8

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cites work

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Incomplete and inaccurate vocal imitation after knockdown of FoxP2 in songbird basal ganglia nucleus Area X.

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7 April 2017

High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders

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PubMed Central

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7 April 2017

Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia

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PubMed Central

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7 April 2017

Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits

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PubMed Central

reference URL

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7 April 2017

Transcriptional and DNA binding activity of the Foxp1/2/4 family is modulated by heterotypic and homotypic protein interactions

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PubMed Central

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7 April 2017

JM2, encoding a fork head-related protein, is mutated in X-linked autoimmunity-allergic disregulation syndrome

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7 April 2017

Foxp2 and Foxp1 cooperatively regulate lung and esophagus development

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PubMed Central

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7 April 2017

A forkhead-domain gene is mutated in a severe speech and language disorder

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PubMed Central

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7 April 2017

FoxP2 expression in avian vocal learners and non-learners

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PubMed Central

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7 April 2017

Parallel FoxP1 and FoxP2 expression in songbird and human brain predicts functional interaction

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Hox repertoires for motor neuron diversity and connectivity gated by a single accessory factor, FoxP1.

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Stereochemical criteria for prediction of the effects of proline mutations on protein stability

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28 September 2017

Functional genetic analysis of mutations implicated in a human speech and language disorder

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28 September 2017

Speech, prosody, and voice characteristics of a mother and daughter with a 7;13 translocation affecting FOXP2.

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28 September 2017

Multiple Domains Define the Expression and Regulatory Properties of Foxp1 Forkhead Transcriptional Repressors

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28 September 2017

Deciphering the genetic basis of speech and language disorders

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28 September 2017

Prevalence of Specific Language Impairment in Kindergarten Children

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28 September 2017

Proline motifs in peptides and their biological processing

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28 September 2017

Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: clinical report and review.

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Crossref

reference URL

https://api.crossref.org/works/10.1038%2FEJHG.2009.43

retrieved

21 January 2018

Identifiers

DOI

10.1038/EJHG.2009.43

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Dimensions Publication ID

1028352710

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PMC publication ID

2784575

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PubMed publication ID

19352412

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ResearchGate publication ID

24263325

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