Loading...
Sex- & Genotype-Specific Differences in Vocalization Development in FMR1 Knockout Mice
Fragile X Syndrome (FXS) is a neurodevelopmental disorder caused by a trinucleotide (CGG) hyperexpansion in the FMR1 gene, functionally silencing transcription of the fragile x mental retardation protein (FMRP). This disorder is characterized by impaired cognition, communication, and social behavior...
Saved in:
| Published in: | Neuroreport |
|---|---|
| Main Authors: | , , , |
| Format: | Artigo |
| Language: | Inglês |
| Published: |
2016
|
| Subjects: | |
| Online Access: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5290539/ https://ncbi.nlm.nih.gov/pubmed/27824730 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/WNR.0000000000000701 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|