| Autor: |
Seelaar, H, Kamphorst, W, Rosso, S M., Azmani, A, Masdjedi, R, de Koning, I, Maat-Kievit, J A., Anar, B, Kaat, L Donker, Breedveld, G J., Dooijes, D, Rozemuller, J M., Bronner, I F., Rizzu, P, Swieten, J C. van |
| Zdroj: |
Neurology (Ovid); October 2008, Vol. 71 Issue: 16 p1220-1226, 7p |
| Abstrakt: |
Frontotemporal dementia (FTD) is the second most common type of presenile dementia and can be distinguished into various clinical variants. The identification of MAPTand GRNdefects and the discovery of the TDP-43 protein in FTD have led to the classification of pathologic and genetic subtypes. In addition to these genetic subtypes, there exist familial forms of FTD with unknown genetic defects. |
| Databáze: |
Supplemental Index |
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