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Fragile X Syndrome

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Fragile X Syndrome (FXS) is a genetic disease due to a CGG trinucleotide expansion, named full mutation (greater than 200 CGG repeats), in the fragile X mental retardation 1 gene locus Xq27.3; which leads to an hypermethylated region in the gene promoter therefore silencing it and lowering the expre...

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Detalles Bibliográficos
Autores principales:	Saldarriaga, Wilmar, Tassone, Flora, González-Teshima, Laura Yuriko, Forero-Forero, Jose Vicente, Ayala-Zapata, Sebastián, Hagerman, Randi
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Universidad del Valle 2014
Materias:	Review Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4350386/ https://www.ncbi.nlm.nih.gov/pubmed/25767309

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