A novel DNA-binding feature of MeCP2 contributes to Rett syndrome

Bibliographic Details
Main Authors: Xin eXu, Lucas ePozzo-Miller
Format: Article
Language:English
Published: Frontiers Media S.A. 2013-05-01
Series:Frontiers in Cellular Neuroscience
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fncel.2013.00064/full
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spelling doaj-21cf5271f5fa4afc9e4b8d3e1e6ea2f82020-11-24T23:51:56ZengFrontiers Media S.A.Frontiers in Cellular Neuroscience1662-51022013-05-01710.3389/fncel.2013.0006452211A novel DNA-binding feature of MeCP2 contributes to Rett syndromeXin eXu0Lucas ePozzo-Miller1The University of Alabama at BirminghamThe University of Alabama at Birminghamhttp://journal.frontiersin.org/Journal/10.3389/fncel.2013.00064/fullAT-Hook MotifsIntellectual DisabilityRett SyndromeMeCP2ATRX
collection DOAJ
language English
format Article
sources DOAJ
author Xin eXu
Lucas ePozzo-Miller
spellingShingle Xin eXu
Lucas ePozzo-Miller
A novel DNA-binding feature of MeCP2 contributes to Rett syndrome
Frontiers in Cellular Neuroscience
AT-Hook Motifs
Intellectual Disability
Rett Syndrome
MeCP2
ATRX
author_facet Xin eXu
Lucas ePozzo-Miller
author_sort Xin eXu
title A novel DNA-binding feature of MeCP2 contributes to Rett syndrome
title_short A novel DNA-binding feature of MeCP2 contributes to Rett syndrome
title_full A novel DNA-binding feature of MeCP2 contributes to Rett syndrome
title_fullStr A novel DNA-binding feature of MeCP2 contributes to Rett syndrome
title_full_unstemmed A novel DNA-binding feature of MeCP2 contributes to Rett syndrome
title_sort novel dna-binding feature of mecp2 contributes to rett syndrome
publisher Frontiers Media S.A.
series Frontiers in Cellular Neuroscience
issn 1662-5102
publishDate 2013-05-01
topic AT-Hook Motifs
Intellectual Disability
Rett Syndrome
MeCP2
ATRX
url http://journal.frontiersin.org/Journal/10.3389/fncel.2013.00064/full
work_keys_str_mv AT xinexu anoveldnabindingfeatureofmecp2contributestorettsyndrome
AT lucasepozzomiller anoveldnabindingfeatureofmecp2contributestorettsyndrome
AT xinexu noveldnabindingfeatureofmecp2contributestorettsyndrome
AT lucasepozzomiller noveldnabindingfeatureofmecp2contributestorettsyndrome
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