A carregar...
Comprehensive Motor Testing in Fmr1-KO Mice Exposes Temporal Defects in Oromotor Coordination
Fragile X syndrome (FXS; MIM #300624), a well-recognized form of inherited human mental retardation is caused, in most cases, by a CGG trinucleotide repeat expansion in the 5′-untranslated region of FMR1, resulting in reduced expression of the fragile X mental retardation protein (FMRP). Clinical fe...
Na minha lista:
| Publicado no: | Behav Neurosci |
|---|---|
| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2011
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4874324/ https://ncbi.nlm.nih.gov/pubmed/22004265 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1037/a0025920 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|