Frequency of GRN-associated cases in a Russian cohort of patients with frontotemporal dementia.

Yuliya Shpilyukova,Ekaterina Fedotova, Natalya Abramycheva, Dinara Grishina, Elizaveta Seliverstova,Sergey Illarioshkin

Alzheimer's & dementia : the journal of the Alzheimer's Association（2021）

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摘要

Presented are the first data of GRN mutation frequency in Russian patients with FTD. The frequency found is comparable to the data described in other populations. The most frequent disease phenotype in GRN mutation carriers is nfvPPA. Two new frameshift mutations in GRN gene were identified.

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