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PSEN2 Thr421Met Mutation in a Patient with Early O

PSEN2 Thr421Met Mutation in a Patient with Early O

Abstract

A novel mutation in the PSEN2 gene, Thr421Met, was identified in a 57-year-old patient with early-onset Alzheimer's disease. This mutation was previously unknown in Korea, highlighting the importance of genetic screening in patients with EOAD. The discovery of this mutation underscores the need for further research into the genetic underpinnings of Alzheimer's disease, particularly in the Korean population.

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
0
Average
Average
Average