Modeling Fragile X Syndrome: Characterizing Fmr1 Gene Knockout Mice across Genotype, Behavior, and Morphology
Objective: Fragile X syndrome (FXS) is a hereditary condition resulting from dynamic mutations in the Fmr1 gene, leading to reduced or absent fragile X mental retardation protein (FMRP). Although molecular genetic diagnostics for FXS have advanced, there is currently a lack of effective clinical tre...
Збережено в:
| Автори: | , , , , , , , , |
|---|---|
| Формат: | Artigo |
| Мова: | Inglês |
| Опубліковано: |
Wolters Kluwer Medknow Publications
2024-09-01
|
| Серія: | Neurological Sciences and Neurophysiology |
| Предмети: | |
| Онлайн доступ: | https://journals.lww.com/10.4103/nsn.nsn_25_24 |
| Теги: |
Немає тегів, Будьте першим, хто поставить тег для цього запису!
|
