(Q24649522)

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Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia

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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

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Simon E Fisher

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Anthony P Monaco

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Kay D MacDermot

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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

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issue

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

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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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Prevalence of Specific Language Impairment in Kindergarten Children

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

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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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