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

Detalles Bibliográficos
Autores principales: Xu, Xin, Pozzo-Miller, Lucas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3648697/
https://www.ncbi.nlm.nih.gov/pubmed/23675316
http://dx.doi.org/10.3389/fncel.2013.00064
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author Xu, Xin
Pozzo-Miller, Lucas
author_facet Xu, Xin
Pozzo-Miller, Lucas
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spelling pubmed-36486972013-05-14 A novel DNA-binding feature of MeCP2 contributes to Rett syndrome Xu, Xin Pozzo-Miller, Lucas Front Cell Neurosci Neuroscience Frontiers Media S.A. 2013-05-09 /pmc/articles/PMC3648697/ /pubmed/23675316 http://dx.doi.org/10.3389/fncel.2013.00064 Text en Copyright © 2013 Xu and Pozzo-Miller. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Neuroscience
Xu, Xin
Pozzo-Miller, Lucas
A novel DNA-binding feature of MeCP2 contributes to Rett syndrome
title 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_short A novel DNA-binding feature of MeCP2 contributes to Rett syndrome
title_sort novel dna-binding feature of mecp2 contributes to rett syndrome
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3648697/
https://www.ncbi.nlm.nih.gov/pubmed/23675316
http://dx.doi.org/10.3389/fncel.2013.00064
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