USF-LVHN SELECT

Activity-dependent aberrations in gene expression and alternative splicing in a mouse model of Rett syndrome.

Publication/Presentation Date

6-5-2018

Abstract

Rett syndrome (RTT) is a severe neurodevelopmental disorder that affects about 1 in 10,000 female live births. The underlying cause of RTT is mutations in the X-linked gene, methyl-CpG-binding protein 2 (

Volume

115

Issue

23

First Page

5363

Last Page

5363

ISSN

1091-6490

Disciplines

Medical Education | Medicine and Health Sciences

PubMedID

29769330

Department(s)

USF-LVHN SELECT Program, USF-LVHN SELECT Program Students

Document Type

Article

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