FOXP1 mutations cause intellectual disability and a recognizable phenotype-Reference-Cited by-同舟云学术

FOXP1 mutations cause intellectual disability and a recognizable phenotype

Published:2013-09-24 Issue:12 Volume:161 Page:3166-3175
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Le Fevre Anna K.¹²,Taylor Sharelle³,Malek Neva H.,Horn Denise⁴,Carr Christopher W.⁵,Abdul-Rahman Omar A.⁶,O'Donnell Sherindan¹,Burgess Trent⁷,Shaw Marie⁸,Gecz Jozef⁸,Bain Nicole⁹,Fagan Kerry⁹¹⁰,Hunter Matthew F.¹¹⁰

Affiliation:

1. Hunter Genetics; Newcastle NSW Australia

2. John Hunter Children's Hospital; Newcastle NSW Australia

3. Core Interventions Occupational Therapy Services; Gosford NSW Australia

4. Institute of Medical Genetics; Charité University of Berlin; Berlin Germany

5. Department of Dermatology; Emory University; Atlanta Georgia

6. Department of Pediatrics; University of Mississippi Medical Center; Jackson Mississippi

7. VCGS Pathology; Melbourne Australia

8. Department of Pediatrics; The University of Adelaide; SA Australia

9. Hunter Area Pathology Service; John Hunter Hospital; Newcastle NSW Australia

10. University of Newcastle; Newcastle NSW Australia

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.36174/fullpdf

Reference50 articles.

1. The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disorders;Bacon;Hum Genet,2012

2. Expression of the FOXP1 transcription factor is strongly associated with inferior survival in patients with diffuse large B-cell lymphoma;Banham;Clin Cancer Res,2005

3. Forkhead transcription factors: Key players in health and disease;Benayoun;Trends Genet,2011

4. The immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX) is caused by mutations of FOXP3;Bennett;Nat Genet,2001

5. The role of the FOXP family of transcription factors in ASD;Bowers;Dis Markers,2012

Cited by 82 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Joint contractures is a recurrent clinical feature of individuals with neurodevelopmental disorder due to FOXP1 likely gene disruptive variants;American Journal of Medical Genetics Part A;2024-06-26

2. Auditory discrimination learning and acoustic cue weighing in female zebra finches with localized FoxP1 knockdowns;Journal of Neurophysiology;2024-05-01

3. Inhibition of phosphodiesterase 10A by MP-10 rescues behavioral deficits and normalizes microglial morphology and synaptic pruning in a mouse model of FOXP1 syndrome;2024-03-05

4. Novel FOXP2 variant associated with speech and language dysfunction in a Chinese family and literature review;Journal of Applied Genetics;2024-02-28

5. Novel FOXP2 Variant Associated with Speech and Language Dysfunction in a Chinese Family and literature review;2024-01-30