A novel c.1468 G > A GRN mutation causes frontotemporal dementia in a Chinese Han family
Abstract Background/purpose GRN mutations act as causative factors in patients with FTD clinical phenotype or FTD pathology and exhibit high clinical heterogeneity. The discovery of these mutations and the analysis of their associations with resembling Alzheimer’s disease should be critical to under...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , , , |
|---|---|
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
BMC
2025-03-01
|
| Σειρά: | European Journal of Medical Research |
| Θέματα: | |
| Διαθέσιμο Online: | https://doi.org/10.1186/s40001-025-02418-5 |
| Ετικέτες: |
Δεν υπάρχουν, Καταχωρήστε ετικέτα πρώτοι!
|