A carregar...

Genome-wide analysis validates aberrant methylation in fragile X syndrome is specific to the FMR1 locus

BACKGROUND: Fragile X syndrome (FXS) is a common form of inherited intellectual disability caused by an expansion of CGG repeats located in the 5(′) untranslated region (UTR) of the FMR1 gene, which leads to hypermethylation and silencing of this locus. Although a dramatic increase in DNA methylatio...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Alisch, Reid S, Wang, Tao, Chopra, Pankaj, Visootsak, Jeannie, Conneely, Karen N, Warren, Stephen T
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3599197/
https://ncbi.nlm.nih.gov/pubmed/23356558
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2350-14-18
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!