A carregar...
Whole genome microarray analysis of gene expression in subjects with fragile X syndrome
PURPOSE: Fragile X syndrome, the most common inherited form of human mental retardation, arises as a consequence of a large expansion of a CGG trinucleotide repeat in 5′ untranslated region of the fragile X mental retardation 1 (FMR1) gene located on the X chromosome. Although the FMR1 gene was clon...
Na minha lista:
| Publicado no: | Genet Med |
|---|---|
| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2007
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5453801/ https://ncbi.nlm.nih.gov/pubmed/17666893 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|