Caricamento...
Fragile X Syndrome: Loss of Local mRNA Regulation Alters Synaptic Development and Function
Fragile X syndrome is the most common inherited form of cognitive deficiency in humans and perhaps the best-understood single cause of autism. A trinucleotide repeat expansion, inactivating the X-linked FMR1 gene, leads to the absence of the fragile X mental retardation protein. FMRP is a selective...
Salvato in:
| Autori principali: | , |
|---|---|
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2008
|
| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3691995/ https://ncbi.nlm.nih.gov/pubmed/18957214 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.neuron.2008.10.004 |
| Tags: |
Aggiungi Tag
Nessun Tag, puoi essere il primo ad aggiungerne! !
|