Association between PSEN1 p.E318G Variant and APOE Polymorphism and Alzheimer Disease in Turkish Patients
Objective: Mutations in the Presenilin-1 (PSEN1) gene have been associated with early-onset familial Alzheimer disease (AD) and these mutations usually exhibit full penetrance. However, the p.E318G variant located at exon 9 of PSEN1 is an exception. This variant is also seen in non-demented controls...
Main Authors: | , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Galenos Yayinevi
2021-06-01
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Series: | Türk Nöroloji Dergisi |
Subjects: | |
Online Access: | https://tjn.org.tr/jvi.aspx?pdir=tjn&plng=eng&un=TJN-22316&look4= |