Delineation of the movement disorders associated withFOXG1mutations: Table 1-Reference-Cited by-同舟云学术

Delineation of the movement disorders associated withFOXG1mutations: Table 1

Published:2016-03-30 Issue:19 Volume:86 Page:1794-1800
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Papandreou Apostolos,Schneider Ruth B.,Augustine Erika F.,Ng Joanne,Mankad Kshitij,Meyer Esther,McTague Amy,Ngoh Adeline,Hemingway Cheryl,Robinson Robert,Varadkar Sophia M.,Kinali Maria,Salpietro Vincenzo,O'Driscoll Margaret C.,Basheer S. Nigel,Webster Richard I.,Mohammad Shekeeb S.,Pula Shpresa,McGowan Marian,Trump Natalie,Jenkins Lucy,Elmslie Frances,Scott Richard H.,Hurst Jane A.,Perez-Duenas Belen,Paciorkowski Alexander R.,Kurian Manju A.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Reference23 articles.

1. FOXG1 Is Responsible for the Congenital Variant of Rett Syndrome

2. FoxG1 Promotes the Survival of Postmitotic Neurons

3. Phenotypic variability in Rett syndrome associated with FOXG1 mutations in females

4. Novel FOXG1 mutations associated with the congenital variant of Rett syndrome

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