FOXP1 haploinsufficiency: Phenotypes beyond behavior and intellectual disability? - Wikidata - awgldk - TriplyDB

FOXP1 haploinsufficiency: Phenotypes beyond behavior and intellectual disability?

FOXP1 haploinsufficiency: Phenotypes beyond behavior and intellectual disability?

http://www.wikidata.org/entity/Q53081210

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Characterization of a recurrent missense mutation in the forkhead DNA-binding domain of FOXP1

P2860

Q58577846-251E1A65-C328-4DD4-B3F4-5F49E91409FA

P2860

FOXP1 haploinsufficiency: Phenotypes beyond behavior and intellectual disability?

http://www.wikidata.org/entity/Q53081210

description

2017 nî lūn-bûn

@nan

2017年の論文

@ja

2017年学术文章

@wuu

2017年学术文章

@zh

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

2017年學術文章

@zh-hant

name

FOXP1 haploinsufficiency: Phenotypes beyond behavior and intellectual disability?

@en

FOXP1 haploinsufficiency: Phenotypes beyond behavior and intellectual disability?

@nl

type

label

FOXP1 haploinsufficiency: Phenotypes beyond behavior and intellectual disability?

@en

FOXP1 haploinsufficiency: Phenotypes beyond behavior and intellectual disability?

@nl

prefLabel

FOXP1 haploinsufficiency: Phenotypes beyond behavior and intellectual disability?

@en

FOXP1 haploinsufficiency: Phenotypes beyond behavior and intellectual disability?

@nl

P1433

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P1433

American Journal of Medical Genetics

P1476

FOXP1 haploinsufficiency: Phenotypes beyond behavior and intellectual disability?

@en

P2093

Angela Myers

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

Anna Lehman

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

Causes Study

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

Christèle du Souich

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

Jill Mwenifumbo

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

Lior Borovik

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

Rosemarie Rupps

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

P2860

Foxp1 coordinates cardiomyocyte proliferation through both cell-autonomous and nonautonomous mechanisms

Structure of the forkhead domain of FOXP2 bound to DNA

De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairment

Down-regulation of the forkhead transcription factor Foxp1 is required for monocyte differentiation and macrophage function

dbSNP: the NCBI database of genetic variation

Nature, nurture, or chance: stochastic gene expression and its consequences

DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources

Absence of a paternally inherited FOXP2 gene in developmental verbal dyspraxia

Interstitial lung disease in children

P304

3172-3181

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scholarly article

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10.1002/AJMG.A.38462

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12

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P478

173

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Cornelius F Boerkoel

P577

2017-09-08T00:00:00Z

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28884888

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P921

haploinsufficiency