Fragile X Syndrome

Mostrar otras versiones (1)

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...

Descripción completa

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

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4350386/
https://www.ncbi.nlm.nih.gov/pubmed/25767309

Ejemplares similares