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

scientific article

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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Sonja C Vernes

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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page(s)

1354-8

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issue

10

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

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7 April 2017

Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia

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

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

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Foxp2 and Foxp1 cooperatively regulate lung and esophagus development

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

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7 April 2017

FoxP2 expression in avian vocal learners and non-learners

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

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

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

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

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Deciphering the genetic basis of speech and language disorders

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Proline motifs in peptides and their biological processing

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

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Crossref

reference URL

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retrieved

21 January 2018

Identifiers

DOI

10.1038/EJHG.2009.43

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Dimensions Publication ID

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ResearchGate publication ID

24263325

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Springer Nature article ID

10.1038/ejhg.2009.43

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

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

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