Autor: Liu, C., Dong, L., Wang, J., Li, J., Huang, X., Lei, D., Mao, C., Chu, S., Sha, L., Xu, Q., Peng, B., Cui, L., Gao, J.
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GRN mutation spectrum and genotype-phenotype correlation in Chinese dementia patients: data from PUMCH dementia cohort
BackgroundMethodsThe GRN mutations, especially of the loss of function type, are causative of frontotemporal dementia (FTD). However, several GRN variants can be found in other neurodegenerative diseases, such as Alzheimer’s disease (AD) and Park…