Fragile X Syndrome

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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Bibliografske podrobnosti
izdano v:Colomb Med (Cali)
Main Authors: Saldarriaga, Wilmar, Tassone, Flora, González-Teshima, Laura Yuriko, Forero-Forero, Jose Vicente, Ayala-Zapata, Sebastián, Hagerman, Randi
Format: Artigo
Jezik:Inglês
Izdano: Universidad del Valle 2014
Teme:
Review Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC4350386/
https://ncbi.nlm.nih.gov/pubmed/25767309
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