טוען...
Astrocytic contributions to synaptic and learning abnormalities in a mouse model of Fragile X Syndrome
BACKGROUND: Fragile X Syndrome (FXS) is the most common type of mental retardation attributable to a single-gene mutation. It is caused by FMR1 gene silencing and the consequent loss of its protein product, Fragile X Mental Retardation Protein (FMRP). Fmr1 global knock out (KO) mice recapitulate man...
שמור ב:
| הוצא לאור ב: | Biol Psychiatry |
|---|---|
| Main Authors: | , , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
2016
|
| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5348290/ https://ncbi.nlm.nih.gov/pubmed/27865451 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.biopsych.2016.08.036 |
| תגים: |
הוספת תג
אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!
|