APOE genetic variability in an Egyptian cohort of PD

APOE genetic variability in an Egyptian cohort of PD

BackgroundThe apolipoprotein E (APOE) gene, encompassing three alleles (ε2, ε3, ε4), is a critical player in lipid metabolism and has been extensively studied for its role in neurodegenerative diseases. This study examines APOE genetic variability and its association with PD in an Egyptian cohort.Me...

Full description

Saved in:
Bibliographic Details
Main Authors: Eman M. Khedr, Martina B. William, Aliaa A. Elhosseiny, Ali Shalash, Gharib Fawi, Mohamed H. Yousef, Shaimaa El-Jaafary, Hamin Lee, Alina Jama, Mohamed Koraym, Asmaa Helmy, Yara Salah, Peter George, Nourelhoda A. Haridy, Samir Nabhan, Agsha Atputhavadivel, Sara Elfarrash, Gaafar Ragab, Mohamed Tharwat Hegazy, Yasmin Elsaid, Asmaa S. Gabr, Nourhan Shebl, Lobna Aly, Nesreen Abdelwahhab, Tamer M. Belal, Nehal A. B. Elsayed, Mohamed El-Gamal, Shimaa Elgamal, Salma Ragab, Jaidaa Mekky, Henry Houlden, Mie Rizig, Mohamed Salama
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-05-01
Series:Frontiers in Neuroscience
Subjects:
Parkinson’s disease
genetics
APOE
KASP
Egyptian
Online Access:https://www.frontiersin.org/articles/10.3389/fnins.2025.1579968/full
Tags: Add Tag
No Tags, Be the first to tag this record!

Internet

https://www.frontiersin.org/articles/10.3389/fnins.2025.1579968/full

Similar Items