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...
Kaydedildi:
| Asıl Yazarlar: | , , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BMC
2025-03-01
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| Seri Bilgileri: | European Journal of Medical Research |
| Konular: | |
| Online Erişim: | https://doi.org/10.1186/s40001-025-02418-5 |
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