Novel GRN mutations in Koreans with Alzheimer ’s disease

Conclusion: Our data suggest that it would be important to re-examine EOAD patients who had been diagnosed when the FTD spectrum was not well described and the causative FTD genes had not yet been identifed. In addition, we propose initially analyzing genes associated with the frst form of suspected dementia and, if the results are negative, studying genes implicated in the other form of dementia.
Source: Molecular and Cellular Toxicology - Category: Cytology Source Type: research