Cellular origins of auditory event-related potential deficits in Rett syndrome.

Abstract:

:Dysfunction in sensory information processing is a hallmark of many neurological disorders, including autism spectrum disorders, schizophrenia and Rett syndrome (RTT). Using mouse models of RTT, a monogenic disorder caused by mutations in MECP2, we found that the large-scale loss of MeCP2 from forebrain GABAergic interneurons led to deficits in auditory event-related potentials and seizure manifestation, whereas the restoration of MeCP2 in specific classes of interneurons ameliorated these deficits.

journal_name

Nat Neurosci

journal_title

Nature neuroscience

authors

Goffin D,Brodkin ES,Blendy JA,Siegel SJ,Zhou Z

doi

10.1038/nn.3710

subject

Has Abstract

pub_date

2014-06-01 00:00:00

pages

804-6

issue

6

eissn

1097-6256

issn

1546-1726

pii

nn.3710

journal_volume

17

pub_type

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