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...

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Bibliographic Details
Main Authors: Gamze Güven, Haşmet Hanağası, Ebba Lohmann, Nihan Erginel Ünaltuna, Rukiye Aslan, Çağla Dönmez, Başar Bilgiç
Format: Article
Language:English
Published: Galenos Yayinevi 2021-06-01
Series:Türk Nöroloji Dergisi
Subjects:
4
Online Access:https://tjn.org.tr/jvi.aspx?pdir=tjn&plng=eng&un=TJN-22316&look4=