Visual impairment in FOXG1-mutated individuals and mice-Reference-Cited by-同舟云学术

Visual impairment in FOXG1-mutated individuals and mice

Published:2016-06 Issue: Volume:324 Page:496-508
ISSN:0306-4522
Container-title:Neuroscience
language:en
Short-container-title:Neuroscience

Author:

Boggio E.M.,Pancrazi L.,Gennaro M.,Lo Rizzo C.,Mari F.,Meloni I.,Ariani F.,Panighini A.,Novelli E.,Biagioni M.,Strettoi E.,Hayek J.,Rufa A.,Pizzorusso T.,Renieri A.,Costa M.

Funder

Telethon

Italian Health Ministry

Publisher

Elsevier BV

Subject

General Neuroscience

Reference54 articles.

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3. Revisiting the phenotype associated with FOXG1 mutations: two novel cases of congenital Rett variant;Bahi-Buisson;Neurogenetics,2010

4. Environmental enrichment extends photoreceptor survival and visual function in a mouse model of retinitis pigmentosa;Barone;PLoS ONE,2012

5. Widespread changes in dendritic and axonal morphology in Mecp2-mutant mouse models of Rett syndrome: evidence for disruption of neuronal networks;Belichenko;J Comp Neurol,2009

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