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.

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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

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