Familial recurrences ofFOXG1-related disorder: Evidence for mosaicism-Reference-Cited by-同舟云学术

Familial recurrences ofFOXG1-related disorder: Evidence for mosaicism

Published:2015-09-14 Issue:12 Volume:167 Page:3096-3102
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

McMahon Kelly Q.¹,Papandreou Apostolos²³⁴,Ma Mandy⁵,Barry Brenda J.⁶,Mirzaa Ghayda M.⁷,Dobyns William B.⁷,Scott Richard H.⁴⁸,Trump Natalie⁸,Kurian Manju A.²³,Paciorkowski Alex R.¹⁹

Affiliation:

1. Department of Neurology; University of Rochester Medical Center; Rochester New York

2. Developmental Neurosciences; UCL-Institute of Child Health; London United Kingdom

3. Department of Neurology; Great Ormond Street Hospital; London United Kingdom

4. Genetics and Genomics Medicine; UCL-Institute of Child Health; London United Kingdom

5. University of Buffalo School of Medicine; Buffalo New York

6. Children's Hospital Boston; Boston Massachusetts

7. Department of Pediatrics; Division of Genetic Medicine; University of Washington; Center for Integrative Brain Research; Seattle Children's Research Institute; Seattle Washington

8. North East Thames Regional Genetics Service; Great Ormond Street Hospital; London United Kingdom

9. Departments of Pediatrics and Biomedical Genetics; Center for Neural Development and Disease; University of Rochester Medical Center; Rochester New York

Funder

National Institutes of Health, National Institute of Neurologic Disorders and Stroke

Actelion

NBIA Disorders association and Child Brain Research

Wellcome Trust Intermediate Clinical Fellowship

Rosetrees Trust and Gracious Heart Charity Foundation

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference30 articles.

1. FOXG1 is responsible for the congenital variant of Rett syndrome;Ariani;Am J Hum Genet,2008