A carregar...
Molecular Advances Leading to Treatment Implications for Fragile X Premutation Carriers
Fragile X syndrome (FXS) is the most common single gene cause of intellectual disability and it is characterized by a CGG expansion of more than 200 repeats in the FMR1 gene, leading to methylation of the promoter and gene silencing. The fragile X premutation, characterized by a 55 to 200 CGG repeat...
Na minha lista:
| Publicado no: | Brain Disord Ther |
|---|---|
| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2014
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4245015/ https://ncbi.nlm.nih.gov/pubmed/25436181 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4172/2168-975X.1000119 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|